A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5532399



Internal ID9626854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77945489..77946560hg38UCSC Ensembl
Outerchr17:77945452..77946610hg38UCSC Ensembl
Innerchr17:75941571..75942642hg19UCSC Ensembl
Outerchr17:75941534..75942692hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676761
Supporting Variants
SamplesNA19347
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5532399
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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