A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840414



Internal ID22615349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85539920..85555412hg38UCSC Ensembl
chr4:86461073..86476565hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3815493
hg1915493
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491080
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840414
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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