A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025407



Internal ID84672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83717780..83717831hg38UCSC Ensembl
chr9:86332695..86332746hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025407
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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