A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039812



Internal ID94266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98152678..98152911hg38UCSC Ensembl
chr10:99912435..99912668hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480057
Supporting Variants
Samples
Known GenesR3HCC1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039812
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.157089


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