U.S. flag

An official website of the United States government

nsv5429576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,968

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 28 studies. See in: genome view    
Submitted genomic26,312,720-26,316,687Question Mark
Overlapping variant regions from other studies: 99 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):26,639,211-26,643,178Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr126,312,72026,316,687
nsv5429576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr126,639,21126,643,178

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902452deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902452Submitted genomicNC_000001.11:g.263
12720_26316687del
GRCh38 (hg38)NC_000001.11Chr126,312,72026,316,687
nssv16902452RemappedPerfectNC_000001.10:g.266
39211_26643178del
GRCh37.p13First PassNC_000001.10Chr126,639,21126,643,178

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)
nssv16902452<0.00116404
Support Center