A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv991249



Internal ID15938519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8392649..8422381hg38UCSC Ensembl
Innerchr4:8394376..8424108hg19UCSC Ensembl
Innerchr4:8445276..8475008hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3829733
hg1929733
hg1829733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593639
Supporting Variants
Samples
Known GenesACOX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv991249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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