A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364035



Internal ID21021588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46977446..46981361hg38UCSC Ensembl
chr3:47018936..47022851hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383916
hg193916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100730
Samples
Known GenesCCDC12, NBEAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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