A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886553



Internal ID22661541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96955425..96957559hg38UCSC Ensembl
chr15:97498655..97500789hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886553
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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