A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012439



Internal ID21921782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5835468..5835636hg38UCSC Ensembl
chr6:5835701..5835869hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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