A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369511



Internal ID21027064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142590285..142591914hg38UCSC Ensembl
chr3:142309127..142310756hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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