A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368912



Internal ID21026465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129339101..129363600hg38UCSC Ensembl
chr3:129057944..129082443hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3824500
hg1924500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5016n223
Supporting Variantsnssv18208939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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