A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710766



Internal ID18662361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129345003..129455467hg38UCSC Ensembl
Innerchr11:129214898..129325362hg19UCSC Ensembl
Innerchr11:128720108..128830572hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38110465
hg19110465
hg18110465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036787
Supporting Variants
Samples
Known GenesBARX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710766
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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