A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059388



Internal ID20626428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231171527..231176343hg38UCSC Ensembl
chr1:231307273..231312089hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg384817
hg194817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325273
Supporting Variants
Samples
Known GenesTRIM67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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