A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357495



Internal ID21015048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185560201..185571800hg38UCSC Ensembl
chr3:185277989..185289588hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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