A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2672n100



Internal ID22788759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101128866..101274822hg38UCSC Ensembl
chr15:101669071..101815027hg19UCSC Ensembl
chr15:99486594..99632550hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38145957
hg19145957
hg18145957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047802, nsv1053855
Samples
Known GenesCHSY1, VIMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2672n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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