A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771074



Internal ID16065030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37739503..37815386hg38UCSC Ensembl
Innerchr11:37761053..37836936hg19UCSC Ensembl
Innerchr11:37717629..37793512hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3875884
hg1975884
hg1875884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554017
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771074
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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