A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174989



Internal ID20742029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14762377..14762851hg38UCSC Ensembl
chr9:14762375..14762849hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422338
Supporting Variants
Samples
Known GenesFREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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