A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043011



Internal ID19132230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31600987..31665086hg38UCSC Ensembl
Innerchr11:31622534..31686634hg19UCSC Ensembl
Innerchr11:31579110..31643210hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3864100
hg1964101
hg1864101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1090n100
Supporting Variantsnssv3514702
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043011
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