A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5692466



Internal ID9654324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80367251..80371707hg38UCSC Ensembl
Outerchr9:80366880..80372077hg38UCSC Ensembl
Innerchr9:82982166..82986622hg19UCSC Ensembl
Outerchr9:82981795..82986992hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659107
Supporting Variants
SamplesNA19384
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5692466
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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