A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900901



Internal ID22676048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85930954..85937758hg38UCSC Ensembl
chr4:86852107..86858911hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg386805
hg196805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418970
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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