A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639348



Internal ID6679442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82010110..82016025hg38UCSC Ensembl
Innerchr16:82010110..82016025hg38UCSC Ensembl
Outerchr16:82009873..82016267hg38UCSC Ensembl
chr16:82043715..82049630hg19UCSC Ensembl
Innerchr16:82043715..82049630hg19UCSC Ensembl
Outerchr16:82043478..82049872hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385916
hg195916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15538033, essv15538034
SamplesHG01767, NA19679
Known GenesSDR42E1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639348
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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