A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449946



Internal ID21107499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113305034..113307091hg38UCSC Ensembl
chr9:116067314..116069371hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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