A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590262



Internal ID18541857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53674..1799230hg38UCSC Ensembl
Innerchr3:95357..1840914hg19UCSC Ensembl
Innerchr3:70357..1815914hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381745557
hg191745558
hg181745558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007015
Supporting Variants
Samples
Known GenesCHL1, CNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590262
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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