A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864799



Internal ID22639734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112229845..112231244hg38UCSC Ensembl
chr9:114992125..114993524hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510802
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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