A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038449



Internal ID19127668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99110100..99151491hg38UCSC Ensembl
Innerchr11:98980830..99022222hg19UCSC Ensembl
Innerchr11:98486040..98527432hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3841392
hg1941393
hg1841393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710722
Samples
Known GenesCNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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