A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031351



Internal ID88600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136897810..136898032hg38UCSC Ensembl
chr9:139792262..139792484hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474655
Supporting Variants
Samples
Known GenesTRAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031351
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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