A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460203



Internal ID238195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85930954..85937759hg38UCSC Ensembl
chr4:86852107..86858912hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg386806
hg196806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951535
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460203
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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