A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457737



Internal ID235775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159188690..159188747hg38UCSC Ensembl
chr6:159609722..159609779hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735299
Samples
Known GenesFNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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