A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367046



Internal ID21024599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148030828..148031318hg38UCSC Ensembl
chr3:147748615..147749105hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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