A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866084



Internal ID22641019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127840363..127842803hg38UCSC Ensembl
chr9:130602642..130605082hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382441
hg192441
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511407
Samples
Known GenesENG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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