A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051672



Internal ID19140891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120368253..120443469hg38UCSC Ensembl
Innerchr11:120238962..120314178hg19UCSC Ensembl
Innerchr11:119744172..119819388hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875217
hg1975217
hg1875217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520608
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051672
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