A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562205



Internal ID16349614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69188811..69200965hg38UCSC Ensembl
Innerchr13:69762943..69775097hg19UCSC Ensembl
Innerchr13:68660944..68673098hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812155
hg1912155
hg1812155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3233n54
Supporting Variantsnssv813690, nssv1175986
SamplesNINDS_114
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562205
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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