A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847989



Internal ID22622924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81983702..82001771hg38UCSC Ensembl
chr9:84598617..84616686hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3818070
hg1918070
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514455
Samples
Known GenesSPATA31D1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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