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nsv4575797

  • 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: 17 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):110,024,128-110,024,128Question Mark
Overlapping variant regions from other studies: 17 SVs from 5 studies. See in: genome view    
Submitted genomic110,461,933-110,461,933Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4575797RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12110,024,128110,024,128
nsv4575797Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr12110,461,933110,461,933

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16003416sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16003416RemappedPerfectNC_000012.12:g.110
024128_110024129in
s315
GRCh38.p12First PassNC_000012.12Chr12110,024,128110,024,128
nssv16003416Submitted genomicNC_000012.11:g.110
461933_110461934in
s315
GRCh37.p13NC_000012.11Chr12110,461,933110,461,933

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)
nssv160034164.6e-005121694
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