A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896284



Internal ID171671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220114815..220120587hg38UCSC Ensembl
chr1:220288157..220293929hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385773
hg195773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449023
Supporting Variants
Samples
Known GenesIARS2, MIR194-1, MIR215, RNU5F-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896284
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002655


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