A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001545



Internal ID18744076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2193998..2269593hg38UCSC Ensembl
Innerchr3:2235682..2311277hg19UCSC Ensembl
Innerchr3:2210682..2286277hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3875596
hg1975596
hg1875596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590369
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)nsv1001545
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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