A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046292



Internal ID19135511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91788410..91865950hg38UCSC Ensembl
Innerchr11:91521576..91599116hg19UCSC Ensembl
Innerchr11:91161224..91238764hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3877541
hg1977541
hg1877541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512404, nssv3710706
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046292
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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