A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561910



Internal ID16002633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63419953..64466355hg38UCSC Ensembl
Innerchr13:63994086..65040487hg19UCSC Ensembl
Innerchr13:62892087..63938488hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg381046403
hg191046402
hg181046402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3192n54
Supporting Variantsnssv812472
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561910
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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