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nsv5528867

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 26 studies. See in: genome view    
Submitted genomic37,425,046-37,425,177Question Mark
Overlapping variant regions from other studies: 137 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):37,915,948-37,916,079Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,425,04637,425,177
nsv5528867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,915,94837,916,079

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723183duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723183Submitted genomicNC_000019.10:g.374
25046_37425177dup
GRCh38 (hg38)NC_000019.10Chr1937,425,04637,425,177
nssv17723183RemappedPerfectNC_000019.9:g.3791
5948_37916079dup
GRCh37.p13First PassNC_000019.9Chr1937,915,94837,916,079

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)
nssv17723183<0.00116404
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