A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078159



Internal ID21987392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188636933..188636933hg38UCSC Ensembl
chr3:188354721..188354721hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541444
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078159
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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