A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2856968



Internal ID15401796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25266172..25337116hg38UCSC Ensembl
Innerchr1:25592663..25663607hg19UCSC Ensembl
Innerchr1:25465250..25536194hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3870945
hg1970945
hg1870945
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513984
Supporting Variants
SamplesNA19160
Known GenesRHD
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2856968
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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