A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387973



Internal ID21045526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27818401..27820600hg38UCSC Ensembl
chr5:27818508..27820707hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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