A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5617898



Internal ID8939519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28692297..28693104hg38UCSC Ensembl
Outerchr17:28692260..28693154hg38UCSC Ensembl
Innerchr17:27019315..27020122hg19UCSC Ensembl
Outerchr17:27019278..27020172hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677614
Supporting Variants
SamplesHG00464
Known GenesSUPT6H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5617898
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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