A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352420



Internal ID21009973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24783705..24813207hg38UCSC Ensembl
chr2:25006574..25036076hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3829503
hg1929503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085559
Samples
Known GenesCENPO, PTRHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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