A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628087



Internal ID21820134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9733909..9736058hg38UCSC Ensembl
chr17:9637226..9639375hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628087
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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