A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413689



Internal ID192979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14855735..14855786hg38UCSC Ensembl
chr10:14897734..14897785hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032023
Samples
Known GenesHSPA14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413689
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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