A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv968098



Internal ID16262054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95958848..96022412hg38UCSC Ensembl
Innerchr3:95677692..95741256hg19UCSC Ensembl
Innerchr3:97160382..97223946hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3863565
hg1963565
hg1863565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591032
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)nssv968098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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