A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662210



Internal ID9928315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85277743..85284290hg38UCSC Ensembl
Outerchr16:85277706..85284340hg38UCSC Ensembl
Innerchr16:85311349..85317896hg19UCSC Ensembl
Outerchr16:85311312..85317946hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386635
hg196635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6287379
SamplesNA19625
Known GenesLINC00311
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662210
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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