A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172787



Internal ID20739827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9142603..9146892hg38UCSC Ensembl
chr8:9000113..9004402hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg384290
hg194290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433061
Supporting Variants
Samples
Known GenesPPP1R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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