A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496853



Internal ID5563738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62902349..62906465hg38UCSC Ensembl
Innerchr16:62902359..62906455hg38UCSC Ensembl
Outerchr16:62902339..62906475hg38UCSC Ensembl
chr16:62936253..62940369hg19UCSC Ensembl
Innerchr16:62936263..62940359hg19UCSC Ensembl
Outerchr16:62936243..62940379hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638805
Supporting Variants
SamplesNA19011
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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