A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615396



Internal ID16056119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128688840..128690033hg38UCSC Ensembl
Innerchr9:131451119..131452312hg19UCSC Ensembl
Innerchr9:130490940..130492133hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12884n54
Supporting Variantsnssv1143229
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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