A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094657



Internal ID21283674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147730754..147734531hg38UCSC Ensembl
Innerchr4:148651905..148655682hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg383778
hg193778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116264
Supporting Variants
Samplessample348
Known GenesARHGAP10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094657
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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