A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620314



Internal ID21812361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18222146..18222267hg38UCSC Ensembl
chr17:18125460..18125581hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620314
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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