A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467423



Internal ID22525314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:63296220..63298297hg38UCSC Ensembl
chr12:63690000..63692077hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467423
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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