A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2678n100



Internal ID22788765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101485777..101615479hg38UCSC Ensembl
chr15:102025982..102155682hg19UCSC Ensembl
chr15:99843505..99973205hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38129703
hg19129701
hg18129701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048223, nsv1052172, nsv1053891, nsv1044722, nsv1035239, nsv1042872, nsv1037107
Samples
Known GenesPCSK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2678n100
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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