A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148327



Internal ID16001513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136561760..136622988hg38UCSC Ensembl
Innerchr9:139456212..139517440hg19UCSC Ensembl
Innerchr9:138576033..138637261hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3861229
hg1961229
hg1861229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615968
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)nssv1148327
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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