A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638845



Internal ID6678942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65164638..65167082hg38UCSC Ensembl
Innerchr16:65164639..65167081hg38UCSC Ensembl
Outerchr16:65164637..65167083hg38UCSC Ensembl
chr16:65198541..65200985hg19UCSC Ensembl
Innerchr16:65198542..65200984hg19UCSC Ensembl
Outerchr16:65198540..65200986hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382445
hg192445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15499388
SamplesHG02102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638845
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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