A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361855



Internal ID21019408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54616236..54622887hg38UCSC Ensembl
chr3:54650263..54656914hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg386652
hg196652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102714
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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