A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687373



Internal ID18985654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46151810hg38UCSC Ensembl
Innerchr8:46847522..47063432hg19UCSC Ensembl
Innerchr8:46966687..47182597hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38215911
hg19215911
hg18215911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028273
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)nssv3687373
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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