A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7565n54



Internal ID22775460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37326534..37439471hg38UCSC Ensembl
chr20:35954937..36067873hg19UCSC Ensembl
chr20:35388351..35501287hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38112938
hg19112937
hg18112937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585954, nsv585955
SamplesHGDP00715
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7565n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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