A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862194



Internal ID22637129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83013657..83016156hg38UCSC Ensembl
chr15:83682409..83684908hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862194
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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