A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293110



Internal ID5941235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75718175..75719634hg38UCSC Ensembl
Innerchr15:75718206..75719604hg38UCSC Ensembl
Outerchr15:75718145..75719665hg38UCSC Ensembl
chr15:76010516..76011975hg19UCSC Ensembl
Innerchr15:76010547..76011945hg19UCSC Ensembl
Outerchr15:76010486..76012006hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636928
Supporting Variants
SamplesNA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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