A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040992



Internal ID95039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103971306..103974682hg38UCSC Ensembl
chr10:105731064..105734440hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383377
hg193377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513198
Supporting Variants
Samples
Known GenesSLK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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