A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv680n100



Internal ID19011048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15600610..15746123hg38UCSC Ensembl
chr10:15642609..15788122hg19UCSC Ensembl
chr10:15682615..15828128hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38145514
hg19145514
hg18145514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053878, nsv1042034
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)dgv680n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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