A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692722



Internal ID18991003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136341809..136423148hg38UCSC Ensembl
Innerchr8:137354052..137435391hg19UCSC Ensembl
Innerchr8:137423234..137504573hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3881340
hg1981340
hg1881340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032454
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)nssv3692722
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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