A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614156



Internal ID16054879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34572769..34663141hg38UCSC Ensembl
Innerchr9:34572767..34663138hg19UCSC Ensembl
Innerchr9:34562767..34653138hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3890373
hg1990372
hg1890372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12659n54
Supporting Variantsnssv1132848
Samples
Known GenesARID3C, CCL27, CNTFR, CNTFR-AS1, DCTN3, GALT, IL11RA, RPP25L, SIGMAR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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