A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630107



Internal ID21822154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58370254..58370405hg38UCSC Ensembl
chr17:56447615..56447766hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024635
Supporting Variants
Samples
Known GenesRNF43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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