A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590371



Internal ID18541966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2221008..2299059hg38UCSC Ensembl
Innerchr3:2262692..2340743hg19UCSC Ensembl
Innerchr3:2237692..2315743hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3878052
hg1978052
hg1878052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008972
Supporting Variants
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590371
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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