A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854927



Internal ID22629862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56066898..56068894hg38UCSC Ensembl
chr15:56359096..56361092hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381997
hg191997
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854927
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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