A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583952



Internal ID18882233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194047718..194123143hg38UCSC Ensembl
Innerchr2:194912442..194987867hg19UCSC Ensembl
Innerchr2:194620687..194696112hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3875426
hg1975426
hg1875426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003264
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)nssv3583952
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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