A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354257



Internal ID22579926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93945684..93948409hg38UCSC Ensembl
chr12:94339460..94342185hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382726
hg192726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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