A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562766



Internal ID16003489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94712121..94713517hg38UCSC Ensembl
Innerchr13:95364375..95365771hg19UCSC Ensembl
Innerchr13:94162376..94163772hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381397
hg191397
hg181397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817533
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)nsv562766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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