A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857589



Internal ID22632524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49885197..49933173hg38UCSC Ensembl
chr10:51093243..51362797hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3847977
hg19269555
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451756
Samples
Known GenesAGAP8, LOC728407, PARG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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