A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396516



Internal ID21054069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104063959..104070477hg38UCSC Ensembl
chr5:103399660..103406178hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg386519
hg196519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5850n223
Supporting Variantsnssv18212615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396516
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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