A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290466



Internal ID20499684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90946062..90946127hg38UCSC Ensembl
chr15:91489292..91489357hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732693
Supporting Variants
Samples
Known GenesUNC45A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290466
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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