A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020757



Internal ID81485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18580004..18587109hg38UCSC Ensembl
chr9:18580002..18587107hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg387106
hg197106
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556424
Supporting Variants
Samples
Known GenesADAMTSL1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020757
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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