A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753746



Internal ID20529606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165678143..165678143hg38UCSC Ensembl
chr6:166091631..166091631hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753746
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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