A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089806



Internal ID21283751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31926923..31930399hg38UCSC Ensembl
Innerchr10:32215851..32219327hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383477
hg193477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116056
Supporting Variants
Samplessample349
Known GenesARHGAP12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089806
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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