A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764887



Internal ID20540747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16950598..16950598hg38UCSC Ensembl
chr6:16950829..16950829hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764887
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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