A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364053



Internal ID22589722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101456228..101458559hg38UCSC Ensembl
chr12:101850006..101852337hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg382332
hg192332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364053
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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