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nsv4573477

  • 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: 25 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):66,427,020-66,427,020Question Mark
Overlapping variant regions from other studies: 25 SVs from 4 studies. See in: genome view    
Submitted genomic65,722,848-65,722,848Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573477RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr566,427,02066,427,020
nsv4573477Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr565,722,84865,722,848

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16062680line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16062680RemappedPerfectNC_000005.10:g.664
27020_66427021ins6
019
GRCh38.p12First PassNC_000005.10Chr566,427,02066,427,020
nssv16062680Submitted genomicNC_000005.9:g.6572
2848_65722849ins60
19
GRCh37.p13NC_000005.9Chr565,722,84865,722,848

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)
nssv160626804.6e-005121694
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