A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095298



Internal ID21407126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:510333..510333hg38UCSC Ensembl
chr17:413573..413573hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648219
Supporting Variants
SamplesHG00512
Known GenesVPS53
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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