A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389362



Internal ID21046915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12101..84700hg38UCSC Ensembl
chr5:12101..84815hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3872600
hg1972715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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