A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8930n54



Internal ID19001106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4412889..4414085hg38UCSC Ensembl
chr4:4414616..4415812hg19UCSC Ensembl
chr4:4465517..4466713hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg381197
hg191197
hg181197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593477, nsv593478
Samples
Known GenesNSG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8930n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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