A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048429



Internal ID100161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83306656..83311714hg38UCSC Ensembl
chr11:83017699..83022757hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048429
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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