A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410891



Internal ID21068444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102672101..102676700hg38UCSC Ensembl
chr5:102007805..102012404hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5849n223
Supporting Variantsnssv18214473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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