A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880877



Internal ID22655848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89464570..89489792hg38UCSC Ensembl
chr15:90007801..90033023hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3825223
hg1925223
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474359
Samples
Known GenesRHCG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880877
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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