A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9669302



Internal ID13068390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67352556..67352575hg38UCSC Ensembl
Innerchr15:67352552..67352579hg38UCSC Ensembl
Outerchr15:67352533..67352598hg38UCSC Ensembl
chr15:67644894..67644913hg19UCSC Ensembl
Innerchr15:67644890..67644917hg19UCSC Ensembl
Outerchr15:67644871..67644936hg19UCSC Ensembl
chr15:65431948..65431967hg18UCSC Ensembl
Innerchr15:65431971..65431944hg18UCSC Ensembl
Outerchr15:65431925..65431990hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3321784
Supporting Variants
SamplesNA07346
Known GenesIQCH
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9669302
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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