A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576964



Internal ID18875245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12013640..12103834hg38UCSC Ensembl
Innerchr2:12153766..12243960hg19UCSC Ensembl
Innerchr2:12071217..12161411hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3890195
hg1990195
hg1890195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999704
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)nssv3576964
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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