A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871990



Internal ID22646928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44795063..44826927hg38UCSC Ensembl
chr22:45190943..45222807hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3831865
hg1931865
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484186
Samples
Known GenesARHGAP8, PRR5-ARHGAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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