A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621088



Internal ID21813135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:121514..123714hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621088
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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