A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043891



Internal ID19133110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55210908hg38UCSC Ensembl
Innerchr11:54720811..54978384hg19UCSC Ensembl
Innerchr11:54477387..54734960hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38257574
hg19257574
hg18257574
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1162n100
Supporting Variantsnssv3506388, nssv3506072, nssv3507212, nssv3522544, nssv3516694, nssv3513765, nssv3510569, nssv3518741, nssv3511619, nssv3511973, nssv3504136, nssv3510906, nssv3513173, nssv3507963
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)nsv1043891
Frequency
Sample Size11257
Observed Gain11
Observed Loss3
Observed Complex0
Frequencyn/a


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