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nsv4540274

  • 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: 10 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):77,065,769-77,065,769Question Mark
Overlapping variant regions from other studies: 9 SVs from 2 studies. See in: genome view    
Submitted genomic76,776,816-76,776,816Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4540274RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1177,065,76977,065,769
nsv4540274Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1176,776,81676,776,816

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15995992insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15995992RemappedPerfectNC_000011.10:g.770
65769_77065770ins5
8
GRCh38.p12First PassNC_000011.10Chr1177,065,76977,065,769
nssv15995992Submitted genomicNC_000011.9:g.7677
6816_76776817ins58
GRCh37.p13NC_000011.9Chr1176,776,81676,776,816

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)
nssv159959924.6e-005121694
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