A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555338



Internal ID15996061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70136867..70137406hg38UCSC Ensembl
Innerchr11:69982973..69983512hg19UCSC Ensembl
Innerchr11:69660621..69661160hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38540
hg19540
hg18540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1993n54
Supporting Variantsnssv778773, nssv778774, nssv778775, nssv778776
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555338
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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