A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851141



Internal ID22626076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68792705..68793804hg38UCSC Ensembl
chr15:69085044..69086143hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471760
Samples
Known GenesANP32A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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