A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561969



Internal ID16349378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64641130..64723662hg38UCSC Ensembl
Innerchr13:65215262..65297794hg19UCSC Ensembl
Innerchr13:64113263..64195795hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3882533
hg1982533
hg1882533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812606
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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