A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755449



Internal ID20531309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130765400..130765400hg38UCSC Ensembl
chr3:130484244..130484244hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755449
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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