A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676685



Internal ID9942790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133495677..133496209hg38UCSC Ensembl
chr9:136360799..136361331hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1384e199
Supporting Variantsessv5618331, essv6014621, essv5609919, essv6381115, essv5939783, essv5870520, essv5675619, essv6106552, essv5880019, essv5956611, essv5920896, essv5973363, essv5737259
SamplesNA20588, NA19920, NA11992, HG01365, HG00236, HG00154, NA20787, NA19655, NA20801, NA19834, NA20786, HG00280, NA19900
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676685
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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