A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563229



Internal ID16350638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112685447..112791908hg38UCSC Ensembl
Innerchr13:113339761..113446222hg19UCSC Ensembl
Innerchr13:112387762..112494223hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38106462
hg19106462
hg18106462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820156
Samples
Known GenesATP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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