A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614154



Internal ID16401563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34023301..34115078hg38UCSC Ensembl
Innerchr9:34023299..34115076hg19UCSC Ensembl
Innerchr9:34013299..34105076hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3891778
hg1991778
hg1891778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132846
Samples
Known GenesDCAF12, UBAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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