A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895288



Internal ID171037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206123455..206123455hg38UCSC Ensembl
chr1:206217876..206217876hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895288
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.191672


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