A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068766



Internal ID21977999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39179488..39179488hg38UCSC Ensembl
chr5:39179590..39179590hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553546
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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