A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636626



Internal ID6676733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58226877..58292657hg38UCSC Ensembl
Innerchr15:58226882..58292653hg38UCSC Ensembl
Outerchr15:58226873..58292662hg38UCSC Ensembl
chr15:58519076..58584856hg19UCSC Ensembl
Innerchr15:58519081..58584852hg19UCSC Ensembl
Outerchr15:58519072..58584861hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865781
hg1965781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260059
SamplesHG00531
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636626
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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