A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175898



Internal ID20742938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20763858..20812407hg38UCSC Ensembl
chr9:20763857..20812406hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3848550
hg1948550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425997
Supporting Variants
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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