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nsv5495660

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
Submitted genomic36,727,875-36,727,947Question Mark
Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):37,020,076-37,020,148Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495660Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1536,727,87536,727,947
nsv5495660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1537,020,07637,020,148

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701968duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701968Submitted genomicNC_000015.10:g.367
27875_36727947dup
GRCh38 (hg38)NC_000015.10Chr1536,727,87536,727,947
nssv17701968RemappedPerfectNC_000015.9:g.3702
0076_37020148dup
GRCh37.p13First PassNC_000015.9Chr1537,020,07637,020,148

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)
nssv17701968<0.00136404
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