A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5419047



Internal ID8396450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17277059..17277295hg38UCSC Ensembl
chr9:17277057..17277293hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666854
Supporting Variants
SamplesNA19470
Known GenesCNTLN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5419047
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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