A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856193



Internal ID22631128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88395021..88398220hg38UCSC Ensembl
chr9:91009936..91013135hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2158n209
Supporting Variantsnssv17514671
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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