A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639462



Internal ID7026242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85322996..85326267hg38UCSC Ensembl
Innerchr16:85322996..85326267hg38UCSC Ensembl
Outerchr16:85322766..85326431hg38UCSC Ensembl
chr16:85356602..85359873hg19UCSC Ensembl
Innerchr16:85356602..85359873hg19UCSC Ensembl
Outerchr16:85356372..85360037hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv551e214
Supporting Variantsessv15552013, essv15552012
SamplesHG03731, NA20890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639462
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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