A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370486



Internal ID21028039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146485114..146513480hg38UCSC Ensembl
chr3:146202901..146231267hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3828367
hg1928367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209706
Samples
Known GenesPLSCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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