A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423713



Internal ID202726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30131339..30131390hg38UCSC Ensembl
chr17:28458357..28458408hg19UCSC Ensembl
Cytoband17q11.2
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 Variantsnssv17712464
Samples
Known GenesNSRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423713
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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