A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1135454



Internal ID15641954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126301..69128184hg38UCSC Ensembl
Innerchr9:71741217..71743100hg19UCSC Ensembl
Innerchr9:70931037..70932920hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381884
hg191884
hg181884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614556
Supporting Variants
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1135454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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