A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141269



Internal ID15647769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114274480..114318108hg38UCSC Ensembl
Innerchr9:117036760..117080388hg19UCSC Ensembl
Innerchr9:116076581..116120209hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3843629
hg1943629
hg1843629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615240
Supporting Variants
Samples
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141269
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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