A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638855



Internal ID7025640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65607349..65608021hg38UCSC Ensembl
Innerchr16:65607352..65608018hg38UCSC Ensembl
Outerchr16:65607346..65608024hg38UCSC Ensembl
chr16:65641252..65641924hg19UCSC Ensembl
Innerchr16:65641255..65641921hg19UCSC Ensembl
Outerchr16:65641249..65641927hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501049, essv15501050, essv15501052, essv15501053, essv15501051
SamplesHG02648, HG02690, HG03986, HG02649, HG04118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638855
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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