A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561904



Internal ID16349313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63395129..63434791hg38UCSC Ensembl
Innerchr13:63969262..64008924hg19UCSC Ensembl
Innerchr13:62867263..62906925hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3839663
hg1939663
hg1839663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3190n54
Supporting Variantsnssv812464, nssv812462, nssv812463
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561904
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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