A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9622n54



Internal ID22777517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17347597..17354556hg38UCSC Ensembl
chr5:17347706..17354665hg19UCSC Ensembl
chr5:17400706..17407665hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386960
hg196960
hg186960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597317, nsv597314, nsv597315, nsv597316
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9622n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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