A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617742



Internal ID21809789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34157874..34157959hg38UCSC Ensembl
chr17:32484893..32484978hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617742
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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