A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555199



Internal ID6262712
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639522
Supporting Variants
SamplesNA19783
Known GenesJPH3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555199
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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