A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3234115



Internal ID22372937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:123661257..123672987hg38UCSC Ensembl
Outerchr8:124673497..124685227hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14280466, nssv14280469, nssv14280470, nssv14280468, nssv14280464, nssv14280467, nssv14280465
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, HG00733, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3234115
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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