A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528567



Internal ID18826848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27422057..27555238hg38UCSC Ensembl
Innerchr14:27891263..28024444hg19UCSC Ensembl
Innerchr14:26961103..27094284hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38133182
hg19133182
hg18133182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047510
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)nssv3528567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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