A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574817



Internal ID21766860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4733648..4736038hg38UCSC Ensembl
chr6:4733882..4736272hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382391
hg192391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019944
Supporting Variants
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574817
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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