U.S. flag

An official website of the United States government

nsv5437479

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,081

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 196 SVs from 34 studies. See in: genome view    
Submitted genomic196,661,903-196,663,983Question Mark
Overlapping variant regions from other studies: 196 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):196,631,033-196,633,113Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437479Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1196,661,903196,663,983
nsv5437479RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1196,631,033196,633,113

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894173deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894173Submitted genomicNC_000001.11:g.196
661903_196663983de
l
GRCh38 (hg38)NC_000001.11Chr1196,661,903196,663,983
nssv16894173RemappedPerfectNC_000001.10:g.196
631033_196633113de
l
GRCh37.p13First PassNC_000001.10Chr1196,631,033196,633,113

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)
nssv16894173<0.00116404
Support Center