A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010140



Internal ID18752671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84947861..84985130hg38UCSC Ensembl
Innerchr3:84997012..85034281hg19UCSC Ensembl
Innerchr3:85079702..85116971hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3837270
hg1937270
hg1837270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596266
Samples
Known GenesCADM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010140
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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