A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141197



Internal ID340392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62958261..63002261hg38UCSC Ensembl
chr6:63668166..63712166hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3844001
hg1944001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141197
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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