A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184116



Internal ID21322912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92630784..92630888hg38UCSC Ensembl
chr15:93174014..93174118hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946635
Supporting Variants
SamplesHG002
Known GenesFAM174B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184116
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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