A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5761n54



Internal ID22773656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71364730..71393760hg38UCSC Ensembl
chr17:69360871..69389901hg19UCSC Ensembl
chr17:66872466..66901496hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3829031
hg1929031
hg1829031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575953, nsv575954
SamplesHGDP00019
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5761n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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