A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875643



Internal ID22650601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111542831..111545872hg38UCSC Ensembl
chr1:112085453..112088494hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg383042
hg193042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362823
Samples
Known GenesADORA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875643
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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