A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855008



Internal ID22629943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103548344..103552116hg38UCSC Ensembl
chr10:105308101..105311873hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464128
Samples
Known GenesNEURL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855008
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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