A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2859005



Internal ID15791934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:44355485..44357093hg38UCSC Ensembl
Innerchr1:44821157..44822765hg19UCSC Ensembl
Innerchr1:44593744..44595352hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381609
hg191609
hg181609
Variant TypeCNV gain
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514926
Supporting Variants
SamplesNA21441
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2859005
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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