A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054766



Internal ID19143985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1946041..2008048hg38UCSC Ensembl
Innerchr11:1967271..2029278hg19UCSC Ensembl
Innerchr11:1923847..1985854hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3862008
hg1962008
hg1862008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1015n100
Supporting Variantsnssv3517836, nssv3506267, nssv3509920, nssv3519212
Samples
Known GenesH19, MIR675, MRPL23, MRPL23-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054766
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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