A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365554



Internal ID21023107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84333294..84510605hg38UCSC Ensembl
chr3:84382445..84559756hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38177312
hg19177312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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