A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141394



Internal ID340590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153420790..153430800hg38UCSC Ensembl
chr6:153741925..153751935hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3810011
hg1910011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141394
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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