A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075163



Internal ID21984396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143126069..143126069hg38UCSC Ensembl
chr3:142844911..142844911hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075163
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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