A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089513



Internal ID21510012
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 StatusS
Merged Variantsnsv5591137
Supporting Variants
SamplesNA20847
Known GenesFAM174B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089513
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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