A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1129328



Internal ID15982514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17506784..17554649hg38UCSC Ensembl
Innerchr9:17506782..17554647hg19UCSC Ensembl
Innerchr9:17496782..17544647hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847866
hg1947866
hg1847866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613700
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)nssv1129328
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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