A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv995n100



Internal ID20152611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132825790..133019278hg38UCSC Ensembl
chr10:134639294..134832782hg19UCSC Ensembl
chr10:134489284..134682772hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38193489
hg19193489
hg18193489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035324, nsv1044835, nsv1049415
Samples
Known GenesLOC399829, TTC40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv995n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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