A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038294



Internal ID19127513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94185671..94249439hg38UCSC Ensembl
Innerchr11:93918837..93982605hg19UCSC Ensembl
Innerchr11:93558485..93622253hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3863769
hg1963769
hg1863769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508407
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)nsv1038294
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer