A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037187



Internal ID18779718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134282136..134340956hg38UCSC Ensembl
Innerchr11:134152030..134210850hg19UCSC Ensembl
Innerchr11:133657240..133716060hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3858821
hg1958821
hg1858821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1302n100
Supporting Variantsnssv3511170, nssv3504125, nssv3522032, nssv3508833, nssv3521294, nssv3710774
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037187
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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