A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140801



Internal ID339994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:60000..144000hg38UCSC Ensembl
chr6:60001..144000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3884001
hg1984000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv417n206
Supporting Variantsnssv16977918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140801
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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