A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857995



Internal ID22632930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110517513..110522202hg38UCSC Ensembl
chr9:113279793..113284482hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384690
hg194690
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n209
Supporting Variantsnssv17510743
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857995
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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