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nsv5963813

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 23 studies. See in: genome view    
Submitted genomic163,177,710-163,177,710Question Mark
Overlapping variant regions from other studies: 160 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):163,598,742-163,598,742Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5963813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6163,177,710163,177,710
nsv5963813RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6163,598,742163,598,742

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17426662insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17426662Submitted genomicNC_000006.12:g.163
177710_163177711in
s200
GRCh38 (hg38)NC_000006.12Chr6163,177,710163,177,710
nssv17426662RemappedPerfectNC_000006.11:g.163
598742_163598743in
s200
GRCh37.p13First PassNC_000006.11Chr6163,598,742163,598,742

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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