A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387324



Internal ID21044877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26520348..26547980hg38UCSC Ensembl
chr5:26520457..26548089hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3827633
hg1927633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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