A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850394



Internal ID22625329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110470899..110476501hg38UCSC Ensembl
chr9:113233179..113238781hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385603
hg195603
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510732
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850394
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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