A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049053



Internal ID19138272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134488690..134849175hg38UCSC Ensembl
Innerchr11:134358584..134719069hg19UCSC Ensembl
Innerchr11:133863794..134224279hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38360486
hg19360486
hg18360486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1308n100
Supporting Variantsnssv3519842
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049053
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