A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639241



Internal ID7026024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79219778..79258687hg38UCSC Ensembl
Innerchr16:79220278..79258187hg38UCSC Ensembl
Outerchr16:79218778..79259687hg38UCSC Ensembl
chr16:79253675..79292584hg19UCSC Ensembl
Innerchr16:79254175..79292084hg19UCSC Ensembl
Outerchr16:79252675..79293584hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3838910
hg1938910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15530811, essv15530809, essv15530810
SamplesHG04186, NA19474, HG00234
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639241
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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