A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041328



Internal ID19130547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25067166..25115199hg38UCSC Ensembl
Innerchr11:25088712..25136745hg19UCSC Ensembl
Innerchr11:25045288..25093321hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3848034
hg1948034
hg1848034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1076n100
Supporting Variantsnssv3511113
Samples
Known GenesLUZP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041328
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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