A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848051



Internal ID22622986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79488451..79491162hg38UCSC Ensembl
chr15:79780793..79783504hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382712
hg192712
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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