A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554075



Internal ID16341484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39051419..39110310hg38UCSC Ensembl
Innerchr11:39072969..39131860hg19UCSC Ensembl
Innerchr11:39029545..39088436hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3858892
hg1958892
hg1858892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n54
Supporting Variantsnssv771156, nssv771155, nssv771157
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554075
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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