A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065720



Internal ID21974953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86293772..86293772hg38UCSC Ensembl
chr5:85589590..85589590hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542378
Samples
Known GenesNBPF22P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065720
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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