A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047372



Internal ID18789903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67744858..67893696hg38UCSC Ensembl
Innerchr11:67512329..67661167hg19UCSC Ensembl
Innerchr11:67268905..67417743hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38148839
hg19148839
hg18148839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518552
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)nsv1047372
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