A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576654



Internal ID18874935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55097140..55118126hg38UCSC Ensembl
Innerchr2:55324276..55345262hg19UCSC Ensembl
Innerchr2:55177780..55198766hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3820987
hg1920987
hg1820987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013316
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)nssv3576654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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