A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024372



Internal ID83985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75203552..75340552hg38UCSC Ensembl
chr9:77818468..77955468hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38137001
hg19137001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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