A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038070



Internal ID19127289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80272296hg38UCSC Ensembl
Innerchr11:79967536..79983340hg19UCSC Ensembl
Innerchr11:79645184..79660988hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3815805
hg1915805
hg1815805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1236n100
Supporting Variantsnssv3502891, nssv3518837, nssv3508337, nssv3506683, nssv3503308, nssv3504207, nssv3504723, nssv3502763, nssv3512172, nssv3515169
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)nsv1038070
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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