A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514543



Internal ID15466179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014874..13017110hg38UCSC Ensembl
Innerchr10:13056874..13059110hg19UCSC Ensembl
Innerchr10:13096880..13099116hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382237
hg192237
hg182237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2769796, nssv2778302, nssv2776365, nssv2772484, nssv2769580, nssv2773595, nssv2771031, nssv2772299, nssv2778125
SamplesNA07056, NA12875, NA10839, NA12813, NA07019, NA12005, NA06985, NA12891, NA06991
Known GenesCCDC3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514543
Frequency
Sample Size2366
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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