A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063865



Internal ID21973098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187718106..187718106hg38UCSC Ensembl
chr3:187435894..187435894hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554183
Samples
Known GenesLOC100131635
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063865
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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