A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054299



Internal ID19143518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54762047..54914139hg38UCSC Ensembl
Innerchr11:51205141..51357233hg19UCSC Ensembl
Innerchr11:51061717..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38152093
hg19152093
hg18152093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1154n100
Supporting Variantsnssv3516693
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054299
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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