A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046945



Internal ID19136164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131319093..131338954hg38UCSC Ensembl
Innerchr11:131188988..131208849hg19UCSC Ensembl
Innerchr11:130694198..130714059hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3819862
hg1919862
hg1819862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510512
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)nsv1046945
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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