U.S. flag

An official website of the United States government

nsv5501490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:902

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Submitted genomic93,684,940-93,685,841Question Mark
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):93,418,106-93,419,007Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1193,684,94093,685,841
nsv5501490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1193,418,10693,419,007

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052082duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052082Submitted genomicNC_000011.10:g.936
84940_93685841dup
GRCh38 (hg38)NC_000011.10Chr1193,684,94093,685,841
nssv17052082RemappedPerfectNC_000011.9:g.9341
8106_93419007dup
GRCh37.p13First PassNC_000011.9Chr1193,418,10693,419,007

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)
nssv170520820.004256404
Support Center