A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051966



Internal ID20619006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153217829..153227188hg38UCSC Ensembl
chr1:153190305..153199664hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389360
hg199360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332806
Supporting Variants
Samples
Known GenesPRR9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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