A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv964n100



Internal ID19011332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101363048..101579801hg38UCSC Ensembl
chr10:103122805..103339558hg19UCSC Ensembl
chr10:103112795..103329548hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38216754
hg19216754
hg18216754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055042, nsv1037610
Samples
Known GenesBTRC, POLL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv964n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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