A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359186



Internal ID22584855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118978083..118978083hg38UCSC Ensembl
chr12:119415888..119415888hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359186
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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