A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366809



Internal ID21024362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189790311..189826318hg38UCSC Ensembl
chr3:189508100..189544107hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3836008
hg1936008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100582
Samples
Known GenesTP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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