A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439978



Internal ID21097531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38323901..38326700hg38UCSC Ensembl
chr9:38323898..38326697hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439978
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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