A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673025



Internal ID9939130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89914167..89914635hg38UCSC Ensembl
chr16:89980575..89981043hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518e199
Supporting Variantsessv5847863, essv6147582, essv6293529, essv6495922
SamplesNA19920, NA19383, HG00152, HG01551
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673025
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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