A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892618



Internal ID19183438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20183714..20418387hg38UCSC Ensembl
Outerchr15:20132782..20418387hg38UCSC Ensembl
Innerchr15:20388967..20623640hg19UCSC Ensembl
Outerchr15:20338035..20623640hg19UCSC Ensembl
Innerchr15:18648981..18883654hg18UCSC Ensembl
Outerchr15:18598049..18883654hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38285606
hg19285606
hg18285606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791655, essv25791817
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892618
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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