A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141299



Internal ID15994485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123345761..123348027hg38UCSC Ensembl
Innerchr9:126108040..126110306hg19UCSC Ensembl
Innerchr9:125147861..125150127hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382267
hg192267
hg182267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615274
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)nssv1141299
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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