A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272702



Internal ID20481920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88901004..88901133hg38UCSC Ensembl
chr15:89444235..89444364hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730855
Supporting Variants
Samples
Known GenesMFGE8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272702
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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