A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670856



Internal ID9936961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78286911..78287871hg38UCSC Ensembl
chr9:80901827..80902787hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6243973, essv6039011
SamplesNA19332, NA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670856
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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