A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15260058



Internal ID5261874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58166501..58173497hg38UCSC Ensembl
Innerchr15:58166505..58173493hg38UCSC Ensembl
Outerchr15:58166497..58173501hg38UCSC Ensembl
chr15:58458700..58465696hg19UCSC Ensembl
Innerchr15:58458704..58465692hg19UCSC Ensembl
Outerchr15:58458696..58465700hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386997
hg196997
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636625
Supporting Variants
SamplesNA19664
Known GenesAQP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15260058
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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