A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378141



Internal ID21035694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20470317..20470926hg38UCSC Ensembl
chr5:20470426..20471035hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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