A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019229



Internal ID21928572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135152610..135158842hg38UCSC Ensembl
chr6:135473748..135479980hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386233
hg196233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019229
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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