A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2858852



Internal ID15432778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:53023468..53024056hg38UCSC Ensembl
Innerchr1:53489140..53489728hg19UCSC Ensembl
Innerchr1:53261728..53262316hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38589
hg19589
hg18589
Variant TypeCNV gain
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514927
Supporting Variants
SamplesNA21359
Known GenesSCP2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2858852
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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