A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858931



Internal ID22633866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131284419..131287940hg38UCSC Ensembl
chr9:134159806..134163327hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383522
hg193522
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858931
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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