A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009451



Internal ID21918794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72472544..72482803hg38UCSC Ensembl
chr5:71768371..71778630hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3810260
hg1910260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541928
Samples
Known GenesZNF366
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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