A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556635



Internal ID16344044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134849175hg38UCSC Ensembl
Innerchr11:134349754..134719069hg19UCSC Ensembl
Innerchr11:133854964..134224279hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38369316
hg19369316
hg18369316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv1176221
Samples1798860280_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556635
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