A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369132



Internal ID21026685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49262995..49266531hg38UCSC Ensembl
chr3:49300428..49303964hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383537
hg193537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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