A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047201



Internal ID99307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75222184..75222297hg38UCSC Ensembl
chr11:74933229..74933342hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008769


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer