A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373075



Internal ID21030628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11905668..11907452hg38UCSC Ensembl
chr3:11947142..11948926hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381785
hg191785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373075
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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