A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2161n209



Internal ID22828236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88469511..88476014hg38UCSC Ensembl
chr9:91084426..91090929hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386504
hg196504
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5859957, nsv5857370
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2161n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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