A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6057656



Internal ID9035059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56860711..56861242hg38UCSC Ensembl
chr17:54938072..54938603hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658087
Supporting Variants
SamplesHG00276
Known GenesDGKE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6057656
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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