A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563149



Internal ID16350558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110913751..110915734hg38UCSC Ensembl
Innerchr13:111566098..111568081hg19UCSC Ensembl
Innerchr13:110364099..110366082hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381984
hg191984
hg181984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819895
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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