A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593378



Internal ID16034101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2249015..2261412hg38UCSC Ensembl
Innerchr4:2250742..2263139hg19UCSC Ensembl
Innerchr4:2220540..2232937hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3812398
hg1912398
hg1812398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8910n54
Supporting Variantsnssv988534
Samples
Known GenesMIR4800, MXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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