A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763407



Internal ID20539267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220418479..220418479hg38UCSC Ensembl
chr1:220591821..220591821hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763407
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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