A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037874



Internal ID92999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92204744..92205669hg38UCSC Ensembl
chr10:93964501..93965426hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475680
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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