A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045388



Internal ID18787919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107816082..107862772hg38UCSC Ensembl
Innerchr11:107686808..107733498hg19UCSC Ensembl
Innerchr11:107192018..107238708hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3846691
hg1946691
hg1846691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1277n100
Supporting Variantsnssv3710747
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045388
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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