A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442800



Internal ID21100353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64062101..64081400hg38UCSC Ensembl
chrUn_gl000211:93654..112953hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3819300
hg1919300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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