A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024349



Internal ID83971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74903041..74903465hg38UCSC Ensembl
chr9:77517957..77518381hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024349
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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