A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742959



Internal ID20518945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141432301..141432364hg38UCSC Ensembl
chr6:141753438..141753501hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742959
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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