A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907670



Internal ID5896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111489646..111489646hg38UCSC Ensembl
chr1:112032268..112032268hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552305
Supporting Variants
Samples
Known GenesADORA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907670
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.148452


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