A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614560



Internal ID16055283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126962..69128184hg38UCSC Ensembl
Innerchr9:71741878..71743100hg19UCSC Ensembl
Innerchr9:70931698..70932920hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381223
hg191223
hg181223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12741n54
Supporting Variantsnssv1135820
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614560
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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