A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046857



Internal ID18789388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55636296hg38UCSC Ensembl
Innerchr11:55361349..55403772hg19UCSC Ensembl
Innerchr11:55117925..55160348hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3842424
hg1942424
hg1842424
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1177n100
Supporting Variantsnssv3505498, nssv3513431, nssv3515064, nssv3507514
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046857
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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