A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389494



Internal ID21047047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36780201..36787900hg38UCSC Ensembl
chr5:36780303..36788002hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5730n223
Supporting Variantsnssv18213418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389494
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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