A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126859



Internal ID15980045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7999346..8016079hg38UCSC Ensembl
Innerchr9:7999346..8016079hg19UCSC Ensembl
Innerchr9:7989346..8006079hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3816734
hg1916734
hg1816734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613271
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)nssv1126859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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