A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910117



Internal ID22685327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88394930..88399215hg38UCSC Ensembl
chr9:91009845..91014130hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg384286
hg194286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2157n209
Supporting Variantsnssv17437970
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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