A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579502



Internal ID18877783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91489004..91741775hg38UCSC Ensembl
Innerchr2:91686694..91929801hg19UCSC Ensembl
Innerchr2:91050421..91293528hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38252772
hg19243108
hg18243108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010328
Supporting Variants
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579502
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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