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nsv5473710

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,826

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 34 studies. See in: genome view    
Submitted genomic96,843,561-96,854,386Question Mark
Overlapping variant regions from other studies: 161 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):96,179,264-96,190,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473710Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr596,843,56196,854,386
nsv5473710RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr596,179,26496,190,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971031deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971031Submitted genomicNC_000005.10:g.968
43561_96854386del
GRCh38 (hg38)NC_000005.10Chr596,843,56196,854,386
nssv16971031RemappedPerfectNC_000005.9:g.9617
9264_96190089del
GRCh37.p13First PassNC_000005.9Chr596,179,26496,190,089

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)
nssv16971031<0.00116404
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