A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593638



Internal ID16034361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8371217..8456667hg38UCSC Ensembl
Innerchr4:8372944..8458394hg19UCSC Ensembl
Innerchr4:8423844..8509294hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3885451
hg1985451
hg1885451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152627
SamplesHGDP00058
Known GenesACOX3, TRMT44
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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