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nsv4269015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 23 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):68,427,016-68,427,091Question Mark
Overlapping variant regions from other studies: 21 SVs from 5 studies. See in: genome view    
Submitted genomic66,423,157-66,423,232Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4269015RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1768,427,01668,427,091
nsv4269015Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1766,423,15766,423,232

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15958026duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15958026RemappedPerfectNC_000017.11:g.684
27016_68427091dup
GRCh38.p12First PassNC_000017.11Chr1768,427,01668,427,091
nssv15958026Submitted genomicNC_000017.10:g.664
23157_66423232dup
GRCh37.p13NC_000017.10Chr1766,423,15766,423,232

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)
nssv15958026<0.001521694
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