A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5589617



Internal ID8567020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133252413..133258230hg38UCSC Ensembl
chr9:136127800..136133621hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385818
hg195822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659903
Supporting Variants
SamplesNA19102
Known GenesABO
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5589617
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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