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nsv4325908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,573

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):139,498,146-139,600,718Question Mark
Overlapping variant regions from other studies: 153 SVs from 18 studies. See in: genome view    
Submitted genomic140,510,389-140,612,961Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4325908RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8139,498,146139,600,718
nsv4325908Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr8140,510,389140,612,961

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090438inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090438RemappedPerfectNC_000008.11:g.139
498146_139600718in
v
GRCh38.p12First PassNC_000008.11Chr8139,498,146139,600,718
nssv16090438Submitted genomicNC_000008.10:g.140
510389_140612961in
v
GRCh37.p13NC_000008.10Chr8140,510,389140,612,961

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)
nssv160904380.01226021694
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