A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6279139



Internal ID9256542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85192793..85201021hg38UCSC Ensembl
Outerchr16:85192756..85201071hg38UCSC Ensembl
Innerchr16:85226399..85234627hg19UCSC Ensembl
Outerchr16:85226362..85234677hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg388316
hg198316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664171
Supporting Variants
SamplesHG00309
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6279139
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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