A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042058



Internal ID19131277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50614043..50810134hg38UCSC Ensembl
Innerchr11:50573214..50769305hg19UCSC Ensembl
Innerchr11:50529790..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38196092
hg19196092
hg18196092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712376
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)nsv1042058
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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