A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022076



Internal ID82381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29080500..29110000hg38UCSC Ensembl
chr9:29080498..29109998hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3829501
hg1929501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142217
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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