A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562765



Internal ID16350174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94711744..94713465hg38UCSC Ensembl
Innerchr13:95363998..95365719hg19UCSC Ensembl
Innerchr13:94161999..94163720hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381722
hg191722
hg181722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3326n54
Supporting Variantsnssv817532
Samples
Known GenesSOX21, SOX21-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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