A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368834



Internal ID21026387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9822707..9824927hg38UCSC Ensembl
chr3:9864391..9866611hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104285
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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