A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593379



Internal ID16034102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2249484..2262496hg38UCSC Ensembl
Innerchr4:2251211..2264223hg19UCSC Ensembl
Innerchr4:2221009..2234021hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3813013
hg1913013
hg1813013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8910n54
Supporting Variantsnssv988535
Samples
Known GenesMIR4800, MXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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