A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2890360



Internal ID15603932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302452..136307220hg38UCSC Ensembl
Innerchr3:136021294..136026062hg19UCSC Ensembl
Innerchr3:137503984..137508752hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384769
hg194769
hg184769
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514170
Supporting Variants
SamplesNA10850
Known GenesPCCB
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2890360
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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