A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12095n54



Internal ID22779990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39367449..39567509hg38UCSC Ensembl
chr8:39224968..39425028hg19UCSC Ensembl
chr8:39344125..39544185hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38200061
hg19200061
hg18200061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611001, nsv610972, nsv610993, nsv611015, nsv610998, nsv610994, nsv611020, nsv610973, nsv611033, nsv611016, nsv611013, nsv610956, nsv611032, nsv611041
Samples
Known GenesADAM3A, ADAM5, LOC100130964
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12095n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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