A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363923



Internal ID21021476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20111608..20112138hg38UCSC Ensembl
chr3:20153100..20153630hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101301
Samples
Known GenesKAT2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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