A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853399



Internal ID22628334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48090469..48092168hg38UCSC Ensembl
chr15:48382666..48384365hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471936, nssv17471937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853399
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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