A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6427465



Internal ID8864687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85208788..85208921hg38UCSC Ensembl
chr16:85242394..85242527hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660336
Supporting Variants
SamplesHG00320
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6427465
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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