A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013565



Internal ID21922908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67824652..68066435hg38UCSC Ensembl
chr5:67120480..67362263hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38241784
hg19241784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013565
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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