A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029971



Internal ID87702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132285681..132285786hg38UCSC Ensembl
chr9:135161068..135161173hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488054
Supporting Variants
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004527


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