A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096616



Internal ID21480524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40490409..40490409hg38UCSC Ensembl
chr17:38646661..38646661hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646439
Supporting Variants
SamplesHG03683
Known GenesTNS4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096616
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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