A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847644



Internal ID22622579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130126309..130132897hg38UCSC Ensembl
chr9:132888588..132895176hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386589
hg196589
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511499
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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