A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5847877



Internal ID9341963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66008304..66018416hg38UCSC Ensembl
chr17:64004422..64014534hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3810113
hg1910113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674176
Supporting Variants
SamplesNA18539
Known GenesCEP112
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5847877
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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