A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664159



Internal ID9930264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129358697..129359142hg38UCSC Ensembl
chr9:132120976..132121421hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5745932, essv5666730, essv6246950, essv6194872, essv5823087, essv5785045, essv6588918
SamplesNA19914, NA19355, NA19190, NA18520, NA18516, NA18909, NA19316
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664159
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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