A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613650



Internal ID16401059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15296121..15378451hg38UCSC Ensembl
Innerchr9:15296119..15378449hg19UCSC Ensembl
Innerchr9:15286119..15368449hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3882331
hg1982331
hg1882331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12573n54
Supporting Variantsnssv1128799
Samples
Known GenesTTC39B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613650
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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