A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639522



Internal ID7026302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87674645..87683487hg38UCSC Ensembl
Innerchr16:87675145..87682987hg38UCSC Ensembl
Outerchr16:87673645..87684487hg38UCSC Ensembl
chr16:87708251..87717093hg19UCSC Ensembl
Innerchr16:87708751..87716593hg19UCSC Ensembl
Outerchr16:87707251..87718093hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388843
hg198843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555199
SamplesNA19783
Known GenesJPH3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639522
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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