A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126860



Internal ID15980046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7999681..8016585hg38UCSC Ensembl
Innerchr9:7999681..8016585hg19UCSC Ensembl
Innerchr9:7989681..8006585hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3816905
hg1916905
hg1816905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613272
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)nssv1126860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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