A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678772



Internal ID9944877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90037301..90040835hg38UCSC Ensembl
chr9:92799583..92803117hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383535
hg193535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6286846
SamplesHG01137
Known GenesLOC286370
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678772
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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