A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076224



Internal ID21985457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130091232..130091232hg38UCSC Ensembl
chr3:129810075..129810075hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557246
Samples
Known GenesALG1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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