A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013100



Internal ID21922443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136475780..136477183hg38UCSC Ensembl
chr5:135811469..135812872hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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