A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593377



Internal ID16380786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2246106..2261919hg38UCSC Ensembl
Innerchr4:2247833..2263646hg19UCSC Ensembl
Innerchr4:2217631..2233444hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3815814
hg1915814
hg1815814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv988533
Samples
Known GenesMIR4800, MXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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