A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712139



Internal ID18663734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20881449..20941810hg38UCSC Ensembl
Innerchr14:21349608..21409969hg19UCSC Ensembl
Innerchr14:20419448..20479809hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3860362
hg1960362
hg1860362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050407
Supporting Variants
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712139
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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