A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850788



Internal ID22625723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124406693..124412743hg38UCSC Ensembl
chr9:127168972..127175022hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511327
Samples
Known GenesPSMB7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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