A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018136



Internal ID21927479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117358812..117359136hg38UCSC Ensembl
chr5:116694508..116694832hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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