A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134082



Internal ID15987268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39437631..39443545hg38UCSC Ensembl
Innerchr9:39437629..39443544hg19UCSC Ensembl
Innerchr9:39427629..39433544hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg385915
hg195916
hg185916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614287
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)nssv1134082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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