A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467485



Internal ID22525376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100256808..100258556hg38UCSC Ensembl
chr12:100650586..100652334hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381749
hg191749
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860659
Supporting Variants
Samples
Known GenesDEPDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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