A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054858



Internal ID19144077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72136751..72169247hg38UCSC Ensembl
Innerchr11:71847797..71880291hg19UCSC Ensembl
Innerchr11:71525445..71557939hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3832497
hg1932495
hg1832495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516767
Samples
Known GenesFOLR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054858
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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