A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907268



Internal ID6269195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88688435..89273883hg19UCSC Ensembl
Outerchr16:88686228..89283809hg19UCSC Ensembl
Innerchr16:87215936..87801384hg18UCSC Ensembl
Outerchr16:87213729..87811310hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1567150
SamplesIS31045
Known GenesACSF3, APRT, CBFA2T3, CDH15, CDT1, CTU2, CYBA, GALNS, IL17C, LINC00304, MGC23284, MIR4722, MVD, PABPN1L, PIEZO1, RNF166, SLC22A31, SNAI3, TRAPPC2L, ZC3H18
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907268
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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