A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062596



Internal ID21971829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106599561..106599561hg38UCSC Ensembl
chr6:107047436..107047436hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563867
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062596
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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