A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362229



Internal ID21019782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38729217..38729789hg38UCSC Ensembl
chr3:38770708..38771280hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100844
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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