A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014711



Internal ID22076342
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156192
Supporting Variants
Samples
Known GenesARHGAP24
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014711
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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