A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893153



Internal ID169592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183702984..183713185hg38UCSC Ensembl
chr1:183672119..183682320hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3810202
hg1910202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439764
Supporting Variants
Samples
Known GenesRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893153
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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