A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510906



Internal ID18809187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55210908hg38UCSC Ensembl
Innerchr11:54720811..54978384hg19UCSC Ensembl
Innerchr11:54477387..54734960hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38257574
hg19257574
hg18257574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043891
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510906
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