A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362736



Internal ID21020289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49395063..49400823hg38UCSC Ensembl
chr3:49432496..49438256hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385761
hg195761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102044
Samples
Known GenesRHOA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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