A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6877n100



Internal ID22792964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6712833..6765164hg38UCSC Ensembl
chr8:6570354..6622685hg19UCSC Ensembl
chr8:6557762..6610095hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3852332
hg1952332
hg1852334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024685, nsv1031063
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6877n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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