A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021361



Internal ID81881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30997464..31001451hg38UCSC Ensembl
chr9:30997462..31001449hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg383988
hg193988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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