A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614555



Internal ID16055278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126301..69128121hg38UCSC Ensembl
Innerchr9:71741217..71743037hg19UCSC Ensembl
Innerchr9:70931037..70932857hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381821
hg191821
hg181821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12739n54
Supporting Variantsnssv1134785, nssv1134781, nssv1134778, nssv1134782, nssv1134783, nssv1134780, nssv1134784, nssv1134779
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614555
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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