A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613144



Internal ID16400553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3061261..3120123hg38UCSC Ensembl
Innerchr9:3061261..3120123hg19UCSC Ensembl
Innerchr9:3051261..3110123hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3858863
hg1958863
hg1858863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126223, nssv1126224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613144
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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