A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989103



Internal ID16283059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2536068..2548745hg38UCSC Ensembl
Innerchr4:2537795..2550472hg19UCSC Ensembl
Innerchr4:2507593..2520270hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3812678
hg1912678
hg1812678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593429
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)nssv989103
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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