A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374862



Internal ID21032415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39112551..39125062hg38UCSC Ensembl
chr3:39154042..39166553hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3812512
hg1912512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100868
Samples
Known GenesTTC21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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