A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364812



Internal ID21022365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94083487..94086604hg38UCSC Ensembl
chr3:93802331..93805448hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106683
Samples
Known GenesNSUN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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