A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15552011



Internal ID5553827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85277814..85284408hg38UCSC Ensembl
Innerchr16:85277864..85284358hg38UCSC Ensembl
Outerchr16:85277764..85284458hg38UCSC Ensembl
chr16:85311420..85318014hg19UCSC Ensembl
Innerchr16:85311470..85317964hg19UCSC Ensembl
Outerchr16:85311370..85318064hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386595
hg196595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639461
Supporting Variants
SamplesNA19625
Known GenesLINC00311
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15552011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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