A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041933



Internal ID18784464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67748292..67969010hg38UCSC Ensembl
Innerchr11:67515763..67736481hg19UCSC Ensembl
Innerchr11:67272339..67493057hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38220719
hg19220719
hg18220719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1219n100
Supporting Variantsnssv3508805
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041933
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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