A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050040



Internal ID101256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95150474..95151029hg38UCSC Ensembl
chr11:94883638..94884193hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050040
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006595


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