A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049998



Internal ID101229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94669107..94672996hg38UCSC Ensembl
chr11:94402273..94406162hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383890
hg193890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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