A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293130



Internal ID5657209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75884892..75885366hg38UCSC Ensembl
Innerchr15:75884893..75885365hg38UCSC Ensembl
Outerchr15:75884891..75885367hg38UCSC Ensembl
chr15:76177233..76177707hg19UCSC Ensembl
Innerchr15:76177234..76177706hg19UCSC Ensembl
Outerchr15:76177232..76177708hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636932
Supporting Variants
SamplesNA19070
Known GenesUBE2Q2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293130
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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