A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024574



Internal ID84116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80890920..80891988hg38UCSC Ensembl
chr9:83505835..83506903hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024574
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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