A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593472



Internal ID16034195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3766595..3768639hg38UCSC Ensembl
Innerchr4:3768322..3770366hg19UCSC Ensembl
Innerchr4:3738120..3740164hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg382045
hg192045
hg182045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8929n54
Supporting Variantsnssv989303
Samples
Known GenesADRA2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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