A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5910822



Internal ID8888225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93064404..93065552hg38UCSC Ensembl
Outerchr9:93064367..93065602hg38UCSC Ensembl
Innerchr9:95826686..95827834hg19UCSC Ensembl
Outerchr9:95826649..95827884hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659260
Supporting Variants
SamplesNA19056
Known GenesSUSD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5910822
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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