A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520380



Internal ID18471975
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 StatusS
Merged Variantsnsv1051445
Supporting Variants
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)nssv3520380
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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