A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360159



Internal ID21017712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142599497..142601092hg38UCSC Ensembl
chr3:142318339..142319934hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381596
hg191596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094358
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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