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nsv4325673

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,556,586

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 9922 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):90,468,977-106,025,562Question Mark
Overlapping variant regions from other studies: 9921 SVs from 23 studies. See in: genome view    
Submitted genomic92,228,734-107,785,320Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4325673RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1090,468,977106,025,562
nsv4325673Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1092,228,734107,785,320

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091235inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091235RemappedPerfectNC_000010.11:g.904
68977_106025562inv
GRCh38.p12First PassNC_000010.11Chr1090,468,977106,025,562
nssv16091235Submitted genomicNC_000010.10:g.922
28734_107785320inv
GRCh37.p13NC_000010.10Chr1092,228,734107,785,320

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)
nssv160912354.6e-005121694
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