A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862541



Internal ID22637476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50890593..50918298hg38UCSC Ensembl
chr15:51182790..51210495hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3827706
hg1927706
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471686
Samples
Known GenesAP4E1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862541
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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