A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451448



Internal ID21109001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66252301..66269700hg38UCSC Ensembl
chr9:42251943..42268712hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817400
hg1916770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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