A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041154



Internal ID18783685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74403756..74466864hg38UCSC Ensembl
Innerchr11:74114801..74177909hg19UCSC Ensembl
Innerchr11:73792449..73855557hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3863109
hg1963109
hg1863109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519029, nssv3506527, nssv3710657
Samples
Known GenesKCNE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041154
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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