A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638158



Internal ID7024944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20847006..20850583hg38UCSC Ensembl
Innerchr16:20847019..20850570hg38UCSC Ensembl
Outerchr16:20846993..20850596hg38UCSC Ensembl
chr16:20858328..20861905hg19UCSC Ensembl
Innerchr16:20858341..20861892hg19UCSC Ensembl
Outerchr16:20858315..20861918hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383578
hg193578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15405429
SamplesNA20539
Known GenesLOC81691
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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