A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141727



Internal ID340924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17000..26000hg38UCSC Ensembl
chr7:17000..26000hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv442n206
Supporting Variantsnssv16990456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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