A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427146



Internal ID22485016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160164390..160165286hg38UCSC Ensembl
chr3:159882177..159883073hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888194
Supporting Variants
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427146
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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