A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7453n54



Internal ID22775348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7404601..7422657hg38UCSC Ensembl
chr20:7385248..7403304hg19UCSC Ensembl
chr20:7333248..7351304hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3818057
hg1918057
hg1818057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585358, nsv585356, nsv585357
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7453n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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