A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603917



Internal ID21552584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81988169..81992901hg38UCSC Ensembl
chr9:84603084..84607816hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384733
hg194733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162689
SamplesHG03065
Known GenesSPATA31D1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603917
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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