A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907968



Internal ID22683178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:35320854..36636674hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381315821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv372n209
Supporting Variantsnssv17368521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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