A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890016



Internal ID167471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145167421..145173546hg38UCSC Ensembl
chr1:149667820..149673967hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg386126
hg196148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416823
Supporting Variants
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890016
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001324


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