A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046075



Internal ID19135294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25067166..25102308hg38UCSC Ensembl
Innerchr11:25088712..25123854hg19UCSC Ensembl
Innerchr11:25045288..25080430hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3835143
hg1935143
hg1835143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1076n100
Supporting Variantsnssv3710062, nssv3710063
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)nsv1046075
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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