A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460528



Internal ID22518411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113138550..113142549hg38UCSC Ensembl
chr12:113576355..113580354hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460528
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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