A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6875n100



Internal ID22792962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6374605..6393413hg38UCSC Ensembl
chr8:6232126..6250934hg19UCSC Ensembl
chr8:6219534..6238342hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818809
hg1918809
hg1818809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021444, nsv1032053
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)dgv6875n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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