A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449399



Internal ID21106952
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 StatusM
Merged Variants
Supporting Variantsnssv18220429
Samples
Known GenesFAM120A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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