A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581119



Internal ID18879400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34521378..34977235hg38UCSC Ensembl
Innerchr2:34746445..35202302hg19UCSC Ensembl
Innerchr2:34599949..35055806hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38455858
hg19455858
hg18455858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003361
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)nssv3581119
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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