A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687322



Internal ID18985603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43628431..43968893hg38UCSC Ensembl
Innerchr8:43483574..43824036hg19UCSC Ensembl
Innerchr8:43602731..43943193hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38340463
hg19340463
hg18340463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017634
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687322
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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