A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128783



Internal ID15981969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14539760..14552238hg38UCSC Ensembl
Innerchr9:14539758..14552236hg19UCSC Ensembl
Innerchr9:14529758..14542236hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3812479
hg1912479
hg1812479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613639
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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