A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15486806



Internal ID5488622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58170015..58172474hg38UCSC Ensembl
Innerchr16:58170515..58171974hg38UCSC Ensembl
Outerchr16:58169015..58173474hg38UCSC Ensembl
chr16:58203919..58206378hg19UCSC Ensembl
Innerchr16:58204419..58205878hg19UCSC Ensembl
Outerchr16:58202919..58207378hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382460
hg192460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638723
Supporting Variants
SamplesHG01686
Known GenesCSNK2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15486806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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