A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902784



Internal ID22677945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85555630..85561358hg38UCSC Ensembl
chr4:86476783..86482511hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg385729
hg195729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417223
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902784
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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