A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128721



Internal ID15981907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13510395..13593126hg38UCSC Ensembl
Innerchr9:13510394..13593125hg19UCSC Ensembl
Innerchr9:13500394..13583125hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3882732
hg1982732
hg1882732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613619
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)nssv1128721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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