A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513198



Internal ID289729
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 StatusM
Merged Variants
Supporting Variantsnssv17040992
Samples
Known GenesSLK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513198
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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