A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514550



Internal ID15466186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275821..28280169hg38UCSC Ensembl
Innerchr10:28564750..28569098hg19UCSC Ensembl
Innerchr10:28604756..28609104hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384349
hg194349
hg184349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2769425, nssv2774742, nssv2771266, nssv2773144, nssv2769047, nssv2769198, nssv2777455, nssv2772409, nssv2768951
SamplesNA19093, NA19149, NA19109, NA18489, NA19108, NA19151, NA18856, NA19094, NA18857
Known GenesMPP7
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514550
Frequency
Sample Size2366
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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