A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852283



Internal ID22627218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114309117..114316405hg38UCSC Ensembl
chr9:117071397..117078685hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387289
hg197289
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510891
Samples
Known GenesCOL27A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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