A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689374



Internal ID21211229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160019925..160019988hg38UCSC Ensembl
chr3:159737712..159737775hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806840
Supporting Variants
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689374
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.758621


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