A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038674



Internal ID18781205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6037473..6069142hg38UCSC Ensembl
Innerchr11:6058703..6090372hg19UCSC Ensembl
Innerchr11:6015279..6046948hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3831670
hg1931670
hg1831670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510324
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)nsv1038674
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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