A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038643



Internal ID19127862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25102193..25272005hg38UCSC Ensembl
Innerchr11:25123739..25293551hg19UCSC Ensembl
Innerchr11:25080315..25250127hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38169813
hg19169813
hg18169813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1077n100
Supporting Variantsnssv3522452, nssv3512872
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)nsv1038643
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer