A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2903361



Internal ID15401805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155673238..155676646hg38UCSC Ensembl
Innerchr4:156594390..156597798hg19UCSC Ensembl
Innerchr4:156813840..156817248hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383409
hg193409
hg183409
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514260
Supporting Variants
SamplesNA19160
Known GenesGUCY1A3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2903361
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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