A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732973



Internal ID20508899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133154306..133154373hg38UCSC Ensembl
chr6:133475445..133475512hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732973
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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