A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050413



Internal ID19139632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34215982..34238273hg38UCSC Ensembl
Innerchr11:34237529..34259820hg19UCSC Ensembl
Innerchr11:34194105..34216396hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3822292
hg1922292
hg1822292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520876
Samples
Known GenesABTB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050413
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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