A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043965



Internal ID97043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42483970..42488626hg38UCSC Ensembl
chr11:42505520..42510176hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384657
hg194657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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