A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688432



Internal ID112098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104887017..104911174hg38UCSC Ensembl
chr11:104757744..104781901hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3824158
hg1924158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497156
Supporting Variants
Samples
Known GenesCASP12, LOC643733
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688432
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