A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896539



Internal ID171839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235097777..235099223hg38UCSC Ensembl
chr1:235261092..235262538hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381447
hg191447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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