A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848361



Internal ID22623296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50153375..50156109hg38UCSC Ensembl
chr12:50547158..50549892hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv410n209
Supporting Variantsnssv17453034, nssv17464692
Samples
Known GenesCERS5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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