A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222287



Internal ID20789327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65721301..65745400hg38UCSC Ensembl
chr9:42702221..42726320hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3824100
hg1924100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438443
Supporting Variants
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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