A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593300



Internal ID16034023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1278876..1318606hg38UCSC Ensembl
Innerchr4:1272664..1312394hg19UCSC Ensembl
Innerchr4:1262664..1302394hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839731
hg1939731
hg1839731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987688
Samples
Known GenesMAEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593300
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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