A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156192



Internal ID22086697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85932114..85936711hg38UCSC Ensembl
Outerchr4:85923197..85938246hg38UCSC Ensembl
Innerchr4:86853267..86857864hg19UCSC Ensembl
Outerchr4:86844350..86859399hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3815050
hg1915050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014711
Samples
Known GenesARHGAP24
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156192
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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