A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840142



Internal ID22615077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85474760..85475883hg38UCSC Ensembl
chr4:86395913..86397036hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497874, nssv17497873
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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