A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12096n54



Internal ID22779991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374115..39483882hg38UCSC Ensembl
chr8:39231634..39341401hg19UCSC Ensembl
chr8:39350791..39460558hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38109768
hg19109768
hg18109768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611026, nsv611025, nsv611027, nsv611005, nsv611019, nsv610959, nsv611022, nsv611003, nsv611018
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12096n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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