A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049157



Internal ID19138376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86698017..86793113hg38UCSC Ensembl
Innerchr11:86409059..86504155hg19UCSC Ensembl
Innerchr11:86086707..86181803hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3895097
hg1995097
hg1895097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519944
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)nsv1049157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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