A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583932



Internal ID21532463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146224821..146224870hg38UCSC Ensembl
chr3:145942608..145942657hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124033
SamplesHG00732
Known GenesPLSCR4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583932
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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