A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039476



Internal ID19128695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55268984hg38UCSC Ensembl
Innerchr11:54720811..55036460hg19UCSC Ensembl
Innerchr11:54477387..54793036hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38315650
hg19315650
hg18315650
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1162n100
Supporting Variantsnssv3503945, nssv3516470, nssv3518828, nssv3510631, nssv3511761, nssv3518333, nssv3511915, nssv3504743, nssv3509600, nssv3508594, nssv3506589, nssv3517234
Samples
Known GenesTRIM48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039476
Frequency
Sample Size11257
Observed Gain10
Observed Loss2
Observed Complex0
Frequencyn/a


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