A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451508



Internal ID21109061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42848715..42866899hg38UCSC Ensembl
chr10:43344163..43362347hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3818185
hg1918185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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