A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5912763



Internal ID8890166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127426251..127427845hg38UCSC Ensembl
Outerchr9:127426214..127427895hg38UCSC Ensembl
Innerchr9:130188530..130190124hg19UCSC Ensembl
Outerchr9:130188493..130190174hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381682
hg191682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665517
Supporting Variants
SamplesHG00143
Known GenesZNF79
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5912763
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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