A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869319



Internal ID22644254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92013297..92019991hg38UCSC Ensembl
chr15:92556527..92563221hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386695
hg196695
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474905
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869319
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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