A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871005



Internal ID6278016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12242759..12245732hg19UCSC Ensembl
Outerchr1:12242458..12246175hg19UCSC Ensembl
Innerchr1:12165346..12168319hg18UCSC Ensembl
Outerchr1:12165045..12168762hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1500665
SamplesSP50179
Known GenesTNFRSF1B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871005
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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