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nsv10764

  • Variant Calls:8
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,996

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):156,046,034-156,068,029Question Mark
Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):155,473,044-155,495,039Question Mark
Submitted genomic155,405,622-155,427,617Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv10764RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5156,046,034156,068,029
nsv10764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5155,473,044155,495,039
nsv10764Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr5155,405,622155,427,617

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15162copy number lossNA18502Oligo aCGHProbe signal intensity703
nssv13652copy number lossNA07029Oligo aCGHProbe signal intensity544
nssv13835copy number lossNA10847Oligo aCGHProbe signal intensity437
nssv13867copy number lossNA11830Oligo aCGHProbe signal intensity568
nssv14343copy number lossNA07048Oligo aCGHProbe signal intensity564
nssv15681copy number lossNA18860Oligo aCGHProbe signal intensity768
nssv15884copy number lossNA18517Oligo aCGHProbe signal intensity698
nssv15192copy number lossNA18502Oligo aCGHProbe signal intensity703

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv15162RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156054172_156054
706)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,054,172156,054,706
nssv13652RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv13835RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv13867RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv14343RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv15681RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv15884RemappedPerfectNC_000005.10:g.(15
6046034_156051396)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,046,034156,051,396156,061,231156,068,029
nssv15192RemappedPerfectNC_000005.10:g.(15
6054172_156054706)
_(156061231_156068
029)del		GRCh38.p12First PassNC_000005.10Chr5156,054,172156,054,706156,061,231156,068,029
nssv15162RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155481182_1554817
16)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,481,182155,481,716
nssv13652RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv13835RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv13867RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv14343RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv15681RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv15884RemappedPerfectNC_000005.9:g.(155
473044_155478406)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,473,044155,478,406155,488,241155,495,039
nssv15192RemappedPerfectNC_000005.9:g.(155
481182_155481716)_
(155488241_1554950
39)del		GRCh37.p13First PassNC_000005.9Chr5155,481,182155,481,716155,488,241155,495,039
nssv15162Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155413760_1554142
94)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,413,760155,414,294
nssv13652Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv13835Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv13867Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv14343Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv15681Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv15884Submitted genomicNC_000005.8:g.(155
405622_155410984)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,405,622155,410,984155,420,819155,427,617
nssv15192Submitted genomicNC_000005.8:g.(155
413760_155414294)_
(155420819_1554276
17)del		NCBI35 (hg17)NC_000005.8Chr5155,413,760155,414,294155,420,819155,427,617

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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