A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874184



Internal ID22649135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89338481..89343639hg38UCSC Ensembl
chr15:89881712..89886870hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874184
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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