A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867683



Internal ID22642618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44819730..44852560hg38UCSC Ensembl
chr22:45215610..45248440hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3832831
hg1932831
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484192, nssv17484191
Samples
Known GenesARHGAP8, PRR5-ARHGAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867683
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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