A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599351



Internal ID21791396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92630786..92630855hg38UCSC Ensembl
chr15:93174016..93174085hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023464
Supporting Variants
Samples
Known GenesFAM174B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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