A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220429



Internal ID20787469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93479138..93484613hg38UCSC Ensembl
chr9:96241420..96246895hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg385476
hg195476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449399
Supporting Variants
Samples
Known GenesFAM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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