A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7648n54



Internal ID22775543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62143364..62144394hg38UCSC Ensembl
chr20:60718420..60719450hg19UCSC Ensembl
chr20:60151815..60152845hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381031
hg191031
hg181031
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586480, nsv586477, nsv586478, nsv586479
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7648n54
Frequency
Sample Size17421
Observed Gain54
Observed Loss17
Observed Complex0
Frequencyn/a


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