A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639309



Internal ID6679404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81086534..81087482hg38UCSC Ensembl
Innerchr16:81086569..81087448hg38UCSC Ensembl
Outerchr16:81086500..81087517hg38UCSC Ensembl
chr16:81120139..81121087hg19UCSC Ensembl
Innerchr16:81120174..81121053hg19UCSC Ensembl
Outerchr16:81120105..81121122hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15535875
SamplesHG02351
Known GenesGCSH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639309
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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