A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160311



Internal ID21475360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129018376..129020003hg38UCSC Ensembl
chr9:131780655..131782282hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602694
Supporting Variants
SamplesHG03371
Known GenesSH3GLB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160311
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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