A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017414



Internal ID21926757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87883005..87884700hg38UCSC Ensembl
chr9:90497920..90499615hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588285
Samples
Known GenesSPATA31E1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017414
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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