A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5643052



Internal ID9624394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90998823..91003674hg38UCSC Ensembl
chr9:93761105..93765956hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668757
Supporting Variants
SamplesNA19334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5643052
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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