A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000130



Internal ID21909473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43367525..43367661hg38UCSC Ensembl
chr5:43367627..43367763hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000130
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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