A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738535



Internal ID162201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124129973..124133557hg38UCSC Ensembl
chr9:126892252..126895836hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383585
hg193585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738535
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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