A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139641



Internal ID338830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143117574..143123574hg38UCSC Ensembl
chr3:142836416..142842416hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940382
Samples
Known GenesCHST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139641
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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