A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363790



Internal ID22589459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92473119..92473119hg38UCSC Ensembl
chr12:92866895..92866895hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363790
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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