A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562756



Internal ID16003479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94526063..94585900hg38UCSC Ensembl
Innerchr13:95178317..95238154hg19UCSC Ensembl
Innerchr13:93976318..94036155hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3859838
hg1959838
hg1859838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817523
Samples
Known GenesTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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