A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034924



Internal ID91007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43926526..43926586hg38UCSC Ensembl
chr10:44421974..44422034hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478389
Supporting Variants
Samples
Known GenesLINC00841
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034924
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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