A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866335



Internal ID22641270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40095924..40121433hg38UCSC Ensembl
chr15:40388125..40413634hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3825510
hg1925510
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471806
Samples
Known GenesBMF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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