A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5656n54



Internal ID20139080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46463467..46529499hg38UCSC Ensembl
chr17:44540833..44606865hg19UCSC Ensembl
chr17:41896148..41962181hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3866033
hg1966033
hg1866034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575374, nsv575373
Samples
Known GenesARL17A, LRRC37A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5656n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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