A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359355



Internal ID22585024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108370131..108371406hg38UCSC Ensembl
chr12:108763908..108765183hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359355
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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