A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871198



Internal ID6278209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103438795..103476179hg19UCSC Ensembl
Outerchr1:103432687..103498029hg19UCSC Ensembl
Innerchr1:103211383..103248767hg18UCSC Ensembl
Outerchr1:103205275..103270617hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1568514
SamplesIS31302
Known GenesCOL11A1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871198
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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