A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453387



Internal ID21110940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13387061..13396054hg38UCSC Ensembl
chr10:13429061..13438054hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388994
hg198994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453387
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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