A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3337124



Internal ID14837395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64368753..64368772hg38UCSC Ensembl
Innerchr15:64368749..64368776hg38UCSC Ensembl
Outerchr15:64368730..64368795hg38UCSC Ensembl
chr15:64660952..64660971hg19UCSC Ensembl
Innerchr15:64660948..64660975hg19UCSC Ensembl
Outerchr15:64660929..64660994hg19UCSC Ensembl
chr15:62448005..62448024hg18UCSC Ensembl
Innerchr15:62448028..62448001hg18UCSC Ensembl
Outerchr15:62447982..62448047hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9669225
SamplesNA19143
Known GenesKIAA0101
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3337124
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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