A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362093



Internal ID21019646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146584801..146586200hg38UCSC Ensembl
chr3:146302588..146303987hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096182
Samples
Known GenesPLSCR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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