A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747446



Internal ID20523464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145367698..145370013hg38UCSC Ensembl
chr6:145688834..145691149hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382316
hg192316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747446
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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