A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841167



Internal ID22616102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143210991..143213053hg38UCSC Ensembl
chr5:142590556..142592618hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382063
hg192063
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495652
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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