A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220482



Internal ID20787522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105266161..105386182hg38UCSC Ensembl
chr9:108028442..108148463hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38120022
hg19120022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454602
Supporting Variants
Samples
Known GenesSLC44A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220482
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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