A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7262n100



Internal ID20158878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86099478..86165139hg38UCSC Ensembl
chr8:87111707..87177368hg19UCSC Ensembl
chr8:87180823..87246484hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3865662
hg1965662
hg1865662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026646, nsv1020115
Samples
Known GenesATP6V0D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7262n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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