A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863848



Internal ID22638783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87078323..87090957hg38UCSC Ensembl
chr9:89693238..89705872hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3812635
hg1912635
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514572
Samples
Known GenesLOC494127
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863848
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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