A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062391



Internal ID21971624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105685306..105685306hg38UCSC Ensembl
chr4:106606463..106606463hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543333
Samples
Known GenesINTS12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062391
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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