A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6876n100



Internal ID20158492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6687977..6812428hg38UCSC Ensembl
chr8:6545498..6669949hg19UCSC Ensembl
chr8:6532906..6657359hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38124452
hg19124452
hg18124454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034115, nsv1030637
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B, XKR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6876n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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