A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859774



Internal ID22634709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113396282..113398781hg38UCSC Ensembl
chr9:116158562..116161061hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510869
Samples
Known GenesALAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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