A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv989n100



Internal ID19011357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128040003..128445808hg38UCSC Ensembl
chr10:129838267..130244072hg19UCSC Ensembl
chr10:129728257..130134062hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38405806
hg19405806
hg18405806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049143, nsv1043925
Samples
Known GenesMKI67, PTPRE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv989n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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