A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv910903



Internal ID6272830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5832209..5840619hg19UCSC Ensembl
Outerchr19:5830447..5841356hg19UCSC Ensembl
Innerchr19:5783209..5791619hg18UCSC Ensembl
Outerchr19:5781447..5792356hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1508266, nssv1502132, nssv1505122
SamplesSP53060, SP51051, SP54635
Known GenesFUT6
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv910903
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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