A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071692



Internal ID21980925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107224031..107224031hg38UCSC Ensembl
chr3:106942878..106942878hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548007
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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