A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041166



Internal ID19130385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15159377..15179720hg38UCSC Ensembl
Innerchr11:15180923..15201266hg19UCSC Ensembl
Innerchr11:15137499..15157842hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3820344
hg1920344
hg1820344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1060n100
Supporting Variantsnssv3510937
Samples
Known GenesINSC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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