A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048154



Internal ID19137373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43005902..43045605hg38UCSC Ensembl
Innerchr11:43027452..43067155hg19UCSC Ensembl
Innerchr11:42984028..43023731hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3839704
hg1939704
hg1839704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510635
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)nsv1048154
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