A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636625



Internal ID6676732
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260057, essv15260058
SamplesNA19664, HG01700
Known GenesAQP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636625
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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