A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140841



Internal ID340035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126145000..126151381hg38UCSC Ensembl
chr4:127066155..127072536hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg386382
hg196382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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