A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6203574



Internal ID9874259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89493597..89496053hg38UCSC Ensembl
chr9:92108512..92110968hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382457
hg192457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657584
Supporting Variants
SamplesNA20582
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6203574
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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