A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639518



Internal ID7026298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87556986..87565230hg38UCSC Ensembl
Innerchr16:87557017..87565200hg38UCSC Ensembl
Outerchr16:87556956..87565261hg38UCSC Ensembl
chr16:87590592..87598836hg19UCSC Ensembl
Innerchr16:87590623..87598806hg19UCSC Ensembl
Outerchr16:87590562..87598867hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388245
hg198245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv553e214
Supporting Variantsessv15555140
SamplesHG00406
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639518
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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