A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593691



Internal ID16034414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10011549..10048517hg38UCSC Ensembl
Innerchr4:10013173..10050141hg19UCSC Ensembl
Innerchr4:9622271..9659239hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3836969
hg1936969
hg1836969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991331
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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