A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754180



Internal ID20530040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93664705..93664705hg38UCSC Ensembl
chr6:94374423..94374423hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754180
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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