A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874633



Internal ID22649587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44807036..44810401hg38UCSC Ensembl
chr22:45202916..45206281hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484188, nssv17484187
Samples
Known GenesARHGAP8, PRR5-ARHGAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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