A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6261288



Internal ID8920258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86596733..86597246hg38UCSC Ensembl
Outerchr16:86596696..86597296hg38UCSC Ensembl
Innerchr16:86630339..86630852hg19UCSC Ensembl
Outerchr16:86630302..86630902hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657383
Supporting Variants
SamplesHG00421
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6261288
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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