A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000202



Internal ID21909545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56288214..56294031hg38UCSC Ensembl
chr5:55584041..55589858hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385818
hg195818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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