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nsv4504630

  • 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: 126 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):112,156,067-112,156,067Question Mark
Overlapping variant regions from other studies: 126 SVs from 7 studies. See in: genome view    
Submitted genomic112,810,381-112,810,381Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4504630RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr13112,156,067112,156,067
nsv4504630Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr13112,810,381112,810,381

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16008327alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16008327RemappedPerfectNC_000013.11:g.112
156067_112156068in
s280
GRCh38.p12First PassNC_000013.11Chr13112,156,067112,156,067
nssv16008327Submitted genomicNC_000013.10:g.112
810381_112810382in
s280
GRCh37.p13NC_000013.10Chr13112,810,381112,810,381

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)
nssv160083274.6e-005121694
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