A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023383



Internal ID83302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72451562..72452155hg38UCSC Ensembl
chr9:75066478..75067071hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023383
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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