A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393567



Internal ID21051120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26772601..26855300hg38UCSC Ensembl
chr5:26772710..26855409hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3882700
hg1982700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5707n223
Supporting Variantsnssv18215747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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