A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059149



Internal ID107302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87967141..87973110hg38UCSC Ensembl
chr11:87678033..87684002hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385970
hg195970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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