A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6113836



Internal ID9091239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20919973..20922448hg38UCSC Ensembl
chr17:20823286..20825761hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674566
Supporting Variants
SamplesNA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6113836
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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