A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448684



Internal ID21106237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120667809..120672807hg38UCSC Ensembl
chr9:123430087..123435085hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384999
hg194999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221002
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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