A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677805



Internal ID9943910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26119520..26124605hg38UCSC Ensembl
chr9:26119518..26124603hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385086
hg195086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6501561
SamplesHG00690
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677805
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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