A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007537



Internal ID18750068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2291083..2342639hg38UCSC Ensembl
Innerchr3:2332767..2384323hg19UCSC Ensembl
Innerchr3:2307767..2359323hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3851557
hg1951557
hg1851557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739545
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)nsv1007537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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