A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043236



Internal ID96534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6120000..6147000hg38UCSC Ensembl
chr11:6141230..6168230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3827001
hg1927001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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