A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576966



Internal ID18875247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12022717..12100896hg38UCSC Ensembl
Innerchr2:12162843..12241022hg19UCSC Ensembl
Innerchr2:12080294..12158473hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3878180
hg1978180
hg1878180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000696
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)nssv3576966
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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