A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871537



Internal ID6278548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12242870..12245732hg19UCSC Ensembl
Outerchr1:12242793..12246175hg19UCSC Ensembl
Innerchr1:12165457..12168319hg18UCSC Ensembl
Outerchr1:12165380..12168762hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1512369
SamplesSP55465
Known GenesTNFRSF1B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871537
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer