A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5885132



Internal ID9163581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92872305..92872441hg38UCSC Ensembl
Outerchr9:92872148..92872594hg38UCSC Ensembl
Innerchr9:95634587..95634723hg19UCSC Ensembl
Outerchr9:95634430..95634876hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671782
Supporting Variants
SamplesHG01359
Known GenesZNF484
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5885132
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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