A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023875



Internal ID83624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86278208..86278244hg38UCSC Ensembl
chr9:88893123..88893159hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544838
Supporting Variants
Samples
Known GenesISCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023875
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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