A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024635



Internal ID21933978
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 StatusM
Merged Variants
Supporting Variantsnssv17630107
Samples
Known GenesRNF43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024635
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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