A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366912



Internal ID21024465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146492777..146502154hg38UCSC Ensembl
chr3:146210564..146219941hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389378
hg199378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096178
Samples
Known GenesPLSCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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