A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001794



Internal ID21911137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148225330..148225408hg38UCSC Ensembl
chr5:147604893..147604971hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001794
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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