U.S. flag

An official website of the United States government

nsv5558680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
Submitted genomic93,736,404-93,736,455Question Mark
Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):93,072,110-93,072,161Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr593,736,40493,736,455
nsv5558680RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,072,11093,072,161

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970401sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970401Submitted genomicNC_000005.10:g.937
36404_93736455ins4
14
GRCh38 (hg38)NC_000005.10Chr593,736,40493,736,455
nssv16970401RemappedPerfectNC_000005.9:g.9307
2110_93072161ins41
4
GRCh37.p13First PassNC_000005.9Chr593,072,11093,072,161

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)
nssv16970401<0.00116404
Support Center