A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367010



Internal ID21024563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103390409..103395751hg38UCSC Ensembl
chr3:103109253..103114595hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg385343
hg195343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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