A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907226



Internal ID6269153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88370667..89035249hg19UCSC Ensembl
Outerchr16:88367063..89046439hg19UCSC Ensembl
Innerchr16:86928168..87562750hg18UCSC Ensembl
Outerchr16:86924564..87573940hg18UCSC 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 Variantsnssv1580923
SamplesIS35484
Known GenesAPRT, CBFA2T3, CDT1, CTU2, CYBA, GALNS, IL17C, MGC23284, MIR4722, MVD, PABPN1L, PIEZO1, RNF166, SNAI3, TRAPPC2L, ZC3H18, ZFPM1, ZNF469
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907226
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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