A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6406177



Internal ID9383580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17401467..17407035hg38UCSC Ensembl
chr9:17401465..17407033hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661216
Supporting Variants
SamplesNA19247
Known GenesCNTLN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6406177
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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