A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999895



Internal ID21909238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42814025..42814137hg38UCSC Ensembl
chr5:42814127..42814239hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999895
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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