A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139525



Internal ID338712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186401634..186401692hg38UCSC Ensembl
chr3:186119423..186119481hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139525
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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