A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2841664



Internal ID15307947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358570..35370838hg38UCSC Ensembl
Innerchr19:35849472..35861740hg19UCSC Ensembl
Innerchr19:40541312..40553580hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812269
hg1912269
hg1812269
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514897
Supporting Variants
SamplesNA12832
Known GenesFFAR3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2841664
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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