A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865325



Internal ID22640260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110393118..110395405hg38UCSC Ensembl
chr9:113155398..113157685hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382288
hg192288
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510716
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865325
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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