A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053896



Internal ID19143115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134997954..135074876hg38UCSC Ensembl
Innerchr11:134867848..134944770hg19UCSC Ensembl
Innerchr11:134373058..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3876923
hg1976923
hg1876925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1320n100
Supporting Variantsnssv3513934, nssv3520988, nssv3515999
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)nsv1053896
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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