A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587425



Internal ID21535985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81921416..81951580hg38UCSC Ensembl
chr9:84536331..84566495hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3830165
hg1930165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162684
SamplesNA20509
Known GenesSPATA31D3, SPATA31D4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587425
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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