A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036581



Internal ID92133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95239129..95239180hg38UCSC Ensembl
chr10:96998886..96998937hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546892
Supporting Variants
Samples
Known GenesPDLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036581
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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