A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011348



Internal ID22072979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77745927..77769759hg38UCSC Ensembl
Outerchr2:77738395..77774182hg38UCSC Ensembl
Innerchr2:77973053..77996885hg19UCSC Ensembl
Outerchr2:77965521..78001308hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3835788
hg1935788
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155739
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011348
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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