A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452799



Internal ID21110352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72247685..72249735hg38UCSC Ensembl
chr10:74007443..74009493hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382051
hg192051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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