A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2889256



Internal ID15346194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:993520..997408hg38UCSC Ensembl
Innerchr3:1035204..1039092hg19UCSC Ensembl
Innerchr3:1010204..1014092hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383889
hg193889
hg183889
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514130
Supporting Variants
SamplesNA18856
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2889256
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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