A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865659



Internal ID22640594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77420437..77431529hg38UCSC Ensembl
chr9:80035353..80046445hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3811093
hg1911093
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514340
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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