A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024123



Internal ID83805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65942145..65959191hg38UCSC Ensembl
chr9:42562141..42579189hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817047
hg1917049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.017921


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