A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066314



Internal ID21975547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47338267..47338267hg38UCSC Ensembl
chr3:47379757..47379757hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538350
Samples
Known GenesKLHL18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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