A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492839



Internal ID270038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24655554..24655623hg38UCSC Ensembl
chr10:24944483..24944552hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032236
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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