A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15530829



Internal ID6096639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79241769..79259665hg38UCSC Ensembl
Innerchr16:79241769..79259665hg38UCSC Ensembl
Outerchr16:79241269..79260165hg38UCSC Ensembl
chr16:79275666..79293562hg19UCSC Ensembl
Innerchr16:79275666..79293562hg19UCSC Ensembl
Outerchr16:79275166..79294062hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3817897
hg1917897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639244
Supporting Variants
SamplesNA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15530829
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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