A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038040



Internal ID18780571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134396901..134547865hg38UCSC Ensembl
Innerchr11:134266795..134417759hg19UCSC Ensembl
Innerchr11:133772005..133922969hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38150965
hg19150965
hg18150965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1307n100
Supporting Variantsnssv3504541
Samples
Known GenesB3GAT1, LOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038040
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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