A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561579



Internal ID16348988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45580614..45633930hg38UCSC Ensembl
Innerchr13:46154749..46208065hg19UCSC Ensembl
Innerchr13:45052750..45106066hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3853317
hg1953317
hg1853317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv810010
Samples
Known GenesFAM194B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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