A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6323839



Internal ID9301242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89351877..89353262hg38UCSC Ensembl
Outerchr16:89351840..89353312hg38UCSC Ensembl
Innerchr16:89418285..89419670hg19UCSC Ensembl
Outerchr16:89418248..89419720hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657359
Supporting Variants
SamplesNA19904
Known GenesANKRD11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6323839
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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