A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049867



Internal ID101138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84411826..84563295hg38UCSC Ensembl
chr11:84122869..84274338hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38151470
hg19151470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496636
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049867
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