A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563150



Internal ID16350559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110913860..110915018hg38UCSC Ensembl
Innerchr13:111566207..111567365hg19UCSC Ensembl
Innerchr13:110364208..110365366hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381159
hg191159
hg181159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819896
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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