A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087137



Internal ID21483894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41614583..41614583hg38UCSC Ensembl
chr17:39770835..39770835hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655461
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087137
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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