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nsv5485515

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:186

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 278 SVs from 37 studies. See in: genome view    
Submitted genomic11,576,127-11,576,312Question Mark
Overlapping variant regions from other studies: 278 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):11,433,636-11,433,821Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485515Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,576,12711,576,312
nsv5485515RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,433,63611,433,821

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008300duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008300Submitted genomicNC_000008.11:g.115
76127_11576312dup
GRCh38 (hg38)NC_000008.11Chr811,576,12711,576,312
nssv17008300RemappedPerfectNC_000008.10:g.114
33636_11433821dup
GRCh37.p13First PassNC_000008.10Chr811,433,63611,433,821

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17008300<0.00116404
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