A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452159



Internal ID21109712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8387208..8467657hg38UCSC Ensembl
chr10:8429171..8509620hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3880450
hg1980450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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