A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019944



Internal ID21929287
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 StatusM
Merged Variants
Supporting Variantsnssv17574817
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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