A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562877



Internal ID16003600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576197..98576994hg38UCSC Ensembl
Innerchr13:99228451..99229248hg19UCSC Ensembl
Innerchr13:98026452..98027249hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38798
hg19798
hg18798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3346n54
Supporting Variantsnssv817787, nssv817786
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562877
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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