A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022178



Internal ID82448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30168689..30264730hg38UCSC Ensembl
chr9:30168687..30264728hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3896042
hg1996042
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022178
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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