A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140645



Internal ID339838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73456490..73464722hg38UCSC Ensembl
chr6:74166213..74174445hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg388233
hg198233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984159
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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