A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371969



Internal ID21029522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184462892..184543283hg38UCSC Ensembl
chr3:184180680..184261071hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3880392
hg1980392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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