A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041197



Internal ID19130416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87474236..87516121hg38UCSC Ensembl
Innerchr11:87185278..87227163hg19UCSC Ensembl
Innerchr11:86862926..86904811hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3841886
hg1941886
hg1841886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710697
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)nsv1041197
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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