A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145118



Internal ID15998304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130193174..130226430hg38UCSC Ensembl
Innerchr9:132955453..132988709hg19UCSC Ensembl
Innerchr9:131995274..132028530hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3833257
hg1933257
hg1833257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615503
Supporting Variants
Samples
Known GenesNCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145118
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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