A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852352



Internal ID22627287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114938160..114940415hg38UCSC Ensembl
chr9:117700440..117702695hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382256
hg192256
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510975, nssv17510974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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