A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062035



Internal ID21971268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40491645..40491645hg38UCSC Ensembl
chr6:40459384..40459384hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564995
Samples
Known GenesLRFN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062035
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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