A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356654



Internal ID22582323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46646612..46646907hg38UCSC Ensembl
chr11:46668162..46668457hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919305
Supporting Variants
Samples
Known GenesATG13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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