A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614552



Internal ID16055275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69122768..69127886hg38UCSC Ensembl
Innerchr9:71737684..71742802hg19UCSC Ensembl
Innerchr9:70927504..70932622hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385119
hg195119
hg185119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134764
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614552
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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