A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051677



Internal ID18794208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133862255..133955026hg38UCSC Ensembl
Innerchr11:133732150..133824921hg19UCSC Ensembl
Innerchr11:133237360..133330131hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3892772
hg1992772
hg1892772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520611
Samples
Known GenesIGSF9B, MIR4697, MIR4697HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051677
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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