A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12103n54



Internal ID22779998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39393511..39507504hg38UCSC Ensembl
chr8:39251030..39365023hg19UCSC Ensembl
chr8:39370187..39484180hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38113994
hg19113994
hg18113994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611029, nsv611030, nsv611038, nsv611035, nsv611036, nsv611047, nsv611034, nsv611037, nsv611028, nsv611046, nsv611045, nsv611039
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12103n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer