A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855101



Internal ID22630036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110579418..110590678hg38UCSC Ensembl
chr9:113341698..113352958hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3811261
hg1911261
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510760, nssv17510761
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer