A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360640



Internal ID21018193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186406590..186415944hg38UCSC Ensembl
chr3:186124379..186133733hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg389355
hg199355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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