A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636483



Internal ID7023277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52104771..52107674hg38UCSC Ensembl
Innerchr15:52104800..52107646hg38UCSC Ensembl
Outerchr15:52104743..52107703hg38UCSC Ensembl
chr15:52396968..52399871hg19UCSC Ensembl
Innerchr15:52396997..52399843hg19UCSC Ensembl
Outerchr15:52396940..52399900hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382904
hg192904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15249302, essv15249303
SamplesHG01054, HG01503
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636483
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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