A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000612



Internal ID21909955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131403356..131408113hg38UCSC Ensembl
chr6:131724496..131729253hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg384758
hg194758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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