A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141297



Internal ID15994483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123343835..123348027hg38UCSC Ensembl
Innerchr9:126106114..126110306hg19UCSC Ensembl
Innerchr9:125145935..125150127hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384193
hg194193
hg184193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615272
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)nssv1141297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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