A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513886



Internal ID18812167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15323999..15368535hg38UCSC Ensembl
Innerchr11:15345545..15390081hg19UCSC Ensembl
Innerchr11:15302121..15346657hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3844537
hg1944537
hg1844537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044103
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)nssv3513886
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