A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764578



Internal ID20540438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20023995..20023995hg38UCSC Ensembl
chr6:20024226..20024226hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764578
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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