A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863295



Internal ID22638230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83650480..83655327hg38UCSC Ensembl
chr15:84319232..84324079hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384848
hg194848
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474289
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863295
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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