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nsv5535791

  • 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: 96 SVs from 27 studies. See in: genome view    
Submitted genomic117,075,955-117,075,955Question Mark
Overlapping variant regions from other studies: 96 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):117,513,760-117,513,760Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535791Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12117,075,955117,075,955
nsv5535791RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12117,513,760117,513,760

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684728insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684728Submitted genomicNC_000012.12:g.117
075955_117075956in
s110
GRCh38 (hg38)NC_000012.12Chr12117,075,955117,075,955
nssv17684728RemappedPerfectNC_000012.11:g.117
513760_117513761in
s110
GRCh37.p13First PassNC_000012.11Chr12117,513,760117,513,760

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)
nssv176847280.0171006048
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