A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883015



Internal ID6290026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147407379..147724086hg19UCSC Ensembl
Outerchr5:147404281..147751035hg19UCSC Ensembl
Innerchr5:147387572..147704279hg18UCSC Ensembl
Outerchr5:147384474..147731228hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1520106
SamplesSP50692
Known GenesSPINK13, SPINK14, SPINK5, SPINK6, SPINK7, SPINK9
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883015
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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