A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404630



Internal ID183979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95274085..95274136hg38UCSC Ensembl
chr10:97033842..97033893hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036585
Samples
Known GenesPDLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404630
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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