A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866774



Internal ID22641709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101721910..101724241hg38UCSC Ensembl
chr9:104484192..104486523hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382332
hg192332
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510375
Samples
Known GenesGRIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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