A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523437



Internal ID18475032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47699622..47751999hg38UCSC Ensembl
Innerchr13:48273757..48326134hg19UCSC Ensembl
Innerchr13:47171758..47224135hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3852378
hg1952378
hg1852378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052701
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)nssv3523437
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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