A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7571n54



Internal ID20140995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41254935..41257465hg38UCSC Ensembl
chr20:39883575..39886105hg19UCSC Ensembl
chr20:39316989..39319519hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg382531
hg192531
hg182531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585988, nsv585987
Samples
Known GenesZHX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7571n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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