A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046540



Internal ID98838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61257449..61267647hg38UCSC Ensembl
chr11:61024921..61035119hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500247
Supporting Variants
Samples
Known GenesVWCE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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