A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024201



Internal ID83870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67320700..67329000hg38UCSC Ensembl
chr9:47265772..47272302hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388301
hg196531
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024201
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.446241


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