A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862149



Internal ID22637084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81125253..81134817hg38UCSC Ensembl
chr15:81417594..81427158hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg389565
hg199565
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474232
Samples
Known GenesC15orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862149
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer