A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591137



Internal ID21539710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92630786..92630854hg38UCSC Ensembl
chr15:93174016..93174084hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089513
SamplesNA20847
Known GenesFAM174B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591137
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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