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nsv5513578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132,907

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 660 SVs from 77 studies. See in: genome view    
Submitted genomic3,598,372-3,731,278Question Mark
Overlapping variant regions from other studies: 660 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):3,619,602-3,752,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5513578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr113,598,3723,731,278
nsv5513578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr113,619,6023,752,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17043122duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17043122Submitted genomicNC_000011.10:g.359
8372_3731278dup
GRCh38 (hg38)NC_000011.10Chr113,598,3723,731,278
nssv17043122RemappedPerfectNC_000011.9:g.3619
602_3752508dup
GRCh37.p13First PassNC_000011.9Chr113,619,6023,752,508

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)
nssv17043122<0.00136404
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