A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033893



Internal ID90297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60955661..60956822hg38UCSC Ensembl
chr10:62715419..62716580hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485805
Supporting Variants
Samples
Known GenesRHOBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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