A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6373435



Internal ID9350838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69163010..69163328hg38UCSC Ensembl
chr9:71777926..71778244hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661677
Supporting Variants
SamplesHG00427
Known GenesTJP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6373435
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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