A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv648n100



Internal ID22786735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26861..157806hg38UCSC Ensembl
chr10:72797..203746hg19UCSC Ensembl
chr10:62797..193746hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38130946
hg19130950
hg18130950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050312, nsv1037682, nsv1054986
Samples
Known GenesTUBB8, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv648n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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