A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614553



Internal ID16055276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126301..69126962hg38UCSC Ensembl
Innerchr9:71741217..71741878hg19UCSC Ensembl
Innerchr9:70931037..70931698hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38662
hg19662
hg18662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134765
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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