A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855378



Internal ID22630313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90807433..90809694hg38UCSC Ensembl
chr12:91201210..91203471hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855378
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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