A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582379



Internal ID18880660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87228690..87725136hg38UCSC Ensembl
Innerchr2:87455813..88024655hg19UCSC Ensembl
Innerchr2:87309324..87805770hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38496447
hg19568843
hg18496447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002857
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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