A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046786



Internal ID99003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65836033..65839371hg38UCSC Ensembl
chr11:65603504..65606842hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383339
hg193339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512656
Supporting Variants
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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