A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616907



Internal ID21808954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89676541..89694249hg38UCSC Ensembl
chr15:90219772..90237480hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3817709
hg1917709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020711
Supporting Variants
Samples
Known GenesPEX11A, PLIN1, WDR93
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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