A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562792



Internal ID16003515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96324091..96911159hg38UCSC Ensembl
Innerchr13:96976345..97563413hg19UCSC Ensembl
Innerchr13:95774346..96361414hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38587069
hg19587069
hg18587069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817574
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562792
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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