A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042715



Internal ID96180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37478280..37478371hg38UCSC Ensembl
chr11:37499830..37499921hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042715
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