A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638743



Internal ID7025528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59229573..59239570hg38UCSC Ensembl
Innerchr16:59229585..59239559hg38UCSC Ensembl
Outerchr16:59229562..59239582hg38UCSC Ensembl
chr16:59263477..59273474hg19UCSC Ensembl
Innerchr16:59263489..59273463hg19UCSC Ensembl
Outerchr16:59263466..59273486hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389998
hg199998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15492254
SamplesHG02025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638743
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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