A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055216



Internal ID20622256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190228396..190232654hg38UCSC Ensembl
chr1:190197526..190201784hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg384259
hg194259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332582
Supporting Variants
Samples
Known GenesBRINP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00111


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