A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012193



Internal ID21921536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79352401..79352522hg38UCSC Ensembl
chr5:78648224..78648345hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012193
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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