A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5653027



Internal ID9877335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59652317..59654328hg38UCSC Ensembl
Outerchr17:59652280..59654378hg38UCSC Ensembl
Innerchr17:57729678..57731689hg19UCSC Ensembl
Outerchr17:57729641..57731739hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg382099
hg192099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672443
Supporting Variants
SamplesNA20588
Known GenesCLTC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5653027
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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