A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9579n54



Internal ID22777474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10562933..10565264hg38UCSC Ensembl
chr5:10563045..10565376hg19UCSC Ensembl
chr5:10616045..10618376hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382332
hg192332
hg182332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597120, nsv597123
Samples
Known GenesANKRD33B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9579n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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