A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162684



Internal ID21508154
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 StatusS
Merged Variantsnsv5587425
Supporting Variants
SamplesNA20509
Known GenesSPATA31D3, SPATA31D4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162684
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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