A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863726



Internal ID22638661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81977013..81993286hg38UCSC Ensembl
chr9:84591928..84608201hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3816274
hg1916274
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514452
Samples
Known GenesSPATA31D1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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