A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445876



Internal ID21103429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66178801..66202700hg38UCSC Ensembl
chr9:42318543..42342576hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3823900
hg1924034
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445876
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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