A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636289



Internal ID6676398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43482105..43482850hg38UCSC Ensembl
Innerchr15:43482113..43482842hg38UCSC Ensembl
Outerchr15:43482097..43482858hg38UCSC Ensembl
chr15:43774303..43775048hg19UCSC Ensembl
Innerchr15:43774311..43775040hg19UCSC Ensembl
Outerchr15:43774295..43775056hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231146
SamplesNA12843
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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