A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023842



Internal ID21933185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74263907..74264162hg38UCSC Ensembl
chr15:74556248..74556503hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612916
Samples
Known GenesCCDC33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023842
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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