A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040640



Internal ID94802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3882322..3885367hg38UCSC Ensembl
chr11:3903552..3906597hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383046
hg193046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512275
Supporting Variants
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040640
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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