A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6711n54



Internal ID22774606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17037822..17060894hg38UCSC Ensembl
chr2:17219089..17242161hg19UCSC Ensembl
chr2:17082570..17105642hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3823073
hg1923073
hg1823073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581070, nsv581068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6711n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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