A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465946



Internal ID22523836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22345011..22347743hg38UCSC Ensembl
chr12:22497945..22500677hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465946
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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