A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871714



Internal ID6278725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12247940..12263817hg19UCSC Ensembl
Outerchr1:12247128..12264223hg19UCSC Ensembl
Innerchr1:12170527..12186404hg18UCSC Ensembl
Outerchr1:12169715..12186810hg18UCSC 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 Variantsnssv1509725
SamplesSP54956
Known GenesMIR4632, TNFRSF1B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871714
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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