A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562147



Internal ID16349556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68368715..68454349hg38UCSC Ensembl
Innerchr13:68942847..69028481hg19UCSC Ensembl
Innerchr13:67840848..67926482hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3885635
hg1985635
hg1885635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175958
SamplesNINDS_158
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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