A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7087n100



Internal ID22793174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13646656..13842119hg38UCSC Ensembl
chr8:13504165..13699628hg19UCSC Ensembl
chr8:13548536..13743999hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38195464
hg19195464
hg18195464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017083, nsv1031939
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7087n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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