A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15492733



Internal ID1075828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59802847..59814174hg38UCSC Ensembl
Innerchr16:59802863..59814158hg38UCSC Ensembl
Outerchr16:59802831..59814190hg38UCSC Ensembl
chr16:59836751..59848078hg19UCSC Ensembl
Innerchr16:59836767..59848062hg19UCSC Ensembl
Outerchr16:59836735..59848094hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811328
hg1911328
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638752
Supporting Variants
SamplesHG00699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15492733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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