A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531232



Internal ID18829513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82973587..83039721hg38UCSC Ensembl
Innerchr14:83439931..83506065hg19UCSC Ensembl
Innerchr14:82509684..82575818hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3866135
hg1966135
hg1866135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035907
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531232
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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