A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001896



Internal ID21911239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154519671..154520297hg38UCSC Ensembl
chr5:153899231..153899857hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001896
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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