A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858817



Internal ID22633752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46733677..46734676hg38UCSC Ensembl
chr15:47025875..47026874hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858817
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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