A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562873



Internal ID16003596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98517173..98596057hg38UCSC Ensembl
Innerchr13:99169427..99248311hg19UCSC Ensembl
Innerchr13:97967428..98046312hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3878885
hg1978885
hg1878885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149455
SamplesHGDP01287
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562873
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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