A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891283



Internal ID168371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156281269..156281376hg38UCSC Ensembl
chr1:156251060..156251167hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433455
Supporting Variants
Samples
Known GenesSMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891283
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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