A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561582



Internal ID16348991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46503311..46530301hg38UCSC Ensembl
Innerchr13:47077446..47104436hg19UCSC Ensembl
Innerchr13:45975447..46002437hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3826991
hg1926991
hg1826991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv810012
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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