A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460437



Internal ID238421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4733640..4736038hg38UCSC Ensembl
chr6:4733874..4736272hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978813
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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