A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861285



Internal ID22636220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49900231..49910098hg38UCSC Ensembl
chr10:51108277..51118144hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg389868
hg199868
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464456
Samples
Known GenesPARG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861285
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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