A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593441



Internal ID16034164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3281695..3340410hg38UCSC Ensembl
Innerchr4:3283422..3342137hg19UCSC Ensembl
Innerchr4:3253220..3311935hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3858716
hg1958716
hg1858716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8923n54
Supporting Variantsnssv1152576
Samples1780854479_A
Known GenesRGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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