A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019687



Internal ID21929030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165997396..165999297hg38UCSC Ensembl
chr5:165424401..165426302hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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