A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059387



Internal ID20626427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231167319..231167625hg38UCSC Ensembl
chr1:231303065..231303371hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327014
Supporting Variants
Samples
Known GenesTRIM67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.1556


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