A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897315



Internal ID6304326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45825894..45834198hg19UCSC Ensembl
Outerchr11:45817637..45838926hg19UCSC Ensembl
Innerchr11:45782470..45790774hg18UCSC Ensembl
Outerchr11:45774213..45795502hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509346
SamplesSP54782
Known GenesSLC35C1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897315
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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