A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv679n100



Internal ID20152295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15529099..15664910hg38UCSC Ensembl
chr10:15571098..15706909hg19UCSC Ensembl
chr10:15611104..15746915hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38135812
hg19135812
hg18135812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039290, nsv1044565, nsv1054400
Samples
Known GenesITGA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv679n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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