A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462916



Internal ID240835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75711936..75724897hg38UCSC Ensembl
chr6:76421652..76434613hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3812962
hg1912962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987302
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462916
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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