A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449238



Internal ID21106791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32518701..32528900hg38UCSC Ensembl
chr9:32518699..32528898hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220616
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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