A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465313



Internal ID243177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75610906..75610995hg38UCSC Ensembl
chr6:76320622..76320711hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987296
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465313
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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