A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619402



Internal ID21811449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11942963..11948294hg38UCSC Ensembl
chr17:11846280..11851611hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385332
hg195332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029024
Supporting Variants
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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