A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051445



Internal ID18793976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134373155..134416469hg38UCSC Ensembl
Innerchr11:134243049..134286363hg19UCSC Ensembl
Innerchr11:133748259..133791573hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3843315
hg1943315
hg1843315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1305n100
Supporting Variantsnssv3520380
Samples
Known GenesB3GAT1, GLB1L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051445
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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