A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018049



Internal ID21927392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141818627..141818803hg38UCSC Ensembl
chr5:141198192..141198368hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018049
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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