U.S. flag

An official website of the United States government

nsv5514950

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,217

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 28 studies. See in: genome view    
Submitted genomic36,519,971-36,522,187Question Mark
Overlapping variant regions from other studies: 146 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):37,010,873-37,013,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514950Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,519,97136,522,187
nsv5514950RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,010,87337,013,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723107deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723107Submitted genomicNC_000019.10:g.365
19971_36522187del
GRCh38 (hg38)NC_000019.10Chr1936,519,97136,522,187
nssv17723107RemappedPerfectNC_000019.9:g.3701
0873_37013089del
GRCh37.p13First PassNC_000019.9Chr1937,010,87337,013,089

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)
nssv17723107<0.00116404
Support Center