A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379813



Internal ID21037366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19215273..19325352hg38UCSC Ensembl
chr5:19215382..19325461hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38110080
hg19110080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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