A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454119



Internal ID21111672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89058984..89059736hg38UCSC Ensembl
chr9:91673899..91674651hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232536
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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