A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089729



Internal ID21270442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27571117..27575111hg38UCSC Ensembl
Innerchr9:27571115..27575109hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383995
hg193995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114226
Supporting Variants
Samplessample150
Known GenesC9orf72
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089729
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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