A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140447



Internal ID339640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19116000..19144000hg38UCSC Ensembl
chr6:19116231..19144231hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140447
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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