A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045130



Internal ID18787661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34620051..34756178hg38UCSC Ensembl
Innerchr11:34641598..34777725hg19UCSC Ensembl
Innerchr11:34598174..34734301hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38136128
hg19136128
hg18136128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1094n100
Supporting Variantsnssv3507945
Samples
Known GenesEHF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045130
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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