A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677829



Internal ID9597248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85281233..85284412hg38UCSC Ensembl
Outerchr16:85281196..85284462hg38UCSC Ensembl
Innerchr16:85314839..85318018hg19UCSC Ensembl
Outerchr16:85314802..85318068hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5462493
SamplesNA19625
Known GenesLINC00311
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677829
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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