A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141016



Internal ID340210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109444790..109450790hg38UCSC Ensembl
chr6:109765993..109771993hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986379
Samples
Known GenesMICAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141016
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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