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nsv4938913

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,141

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
Submitted genomic140,635,007-140,636,196Question Mark
Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):140,014,592-140,015,781Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4938913Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,635,033 (-26, +26)140,636,173 (-23, +23)
nsv4938913RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,014,618 (-26, +26)140,015,758 (-23, +23)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16471390deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16471390Submitted genomicNC_000005.10:g.(14
0635007_140635059)
_(140636150_140636
196)del
GRCh38 (hg38)NC_000005.10Chr5140,635,033 (-26, +26)140,636,173 (-23, +23)
nssv16471390RemappedPerfectNC_000005.9:g.(140
014592_140014644)_
(140015735_1400157
81)del
GRCh37.p13First PassNC_000005.9Chr5140,014,618 (-26, +26)140,015,758 (-23, +23)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16471390<0.001129246
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