A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866030



Internal ID22640965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49928993..49948874hg38UCSC Ensembl
chr10:51137039..51378209hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3819882
hg19241171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450298
Samples
Known GenesAGAP8, LOC728407, PARG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866030
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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