A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053222



Internal ID19142441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15159377..15175514hg38UCSC Ensembl
Innerchr11:15180923..15197060hg19UCSC Ensembl
Innerchr11:15137499..15153636hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3816138
hg1916138
hg1816138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1060n100
Supporting Variantsnssv3522063
Samples
Known GenesINSC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053222
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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