A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100440



Internal ID21458314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9657304..9657304hg38UCSC Ensembl
chr17:9560621..9560621hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659548
Supporting Variants
SamplesHG02587
Known GenesUSP43
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100440
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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