A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556443



Internal ID15997166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113038133..113080060hg38UCSC Ensembl
Innerchr11:112908855..112950782hg19UCSC Ensembl
Innerchr11:112414065..112455992hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3841928
hg1941928
hg1841928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174955
SamplesNINDS_69
Known GenesNCAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556443
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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