A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004393



Internal ID21913736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150572781..150572911hg38UCSC Ensembl
chr5:149952343..149952473hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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