A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639415



Internal ID6679508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84214895..84221460hg38UCSC Ensembl
Innerchr16:84214902..84221454hg38UCSC Ensembl
Outerchr16:84214889..84221467hg38UCSC Ensembl
chr16:84248501..84255066hg19UCSC Ensembl
Innerchr16:84248508..84255060hg19UCSC Ensembl
Outerchr16:84248495..84255073hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386566
hg196566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545801, essv15545800, essv15545802
SamplesNA21123, NA20800, HG03009
Known GenesKCNG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639415
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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