A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220653



Internal ID20787693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93009224..93012115hg38UCSC Ensembl
chr9:95771506..95774397hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382892
hg192892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449719
Supporting Variants
Samples
Known GenesFGD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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