A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132847



Internal ID15639347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34552439..34661997hg38UCSC Ensembl
Innerchr9:34552437..34661994hg19UCSC Ensembl
Innerchr9:34542437..34651994hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38109559
hg19109558
hg18109558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614155
Supporting Variants
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)nssv1132847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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