A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041882



Internal ID95619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:506000..596000hg38UCSC Ensembl
chr11:506000..596000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3890001
hg1990001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143351
Supporting Variants
Samples
Known GenesC11orf35, HRAS, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, RNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.019976


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