A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850212



Internal ID22625147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30388009..30390638hg38UCSC Ensembl
chr13:30962146..30964775hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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