A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8907n54



Internal ID22776802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2058728..2060010hg38UCSC Ensembl
chr4:2060455..2061737hg19UCSC Ensembl
chr4:2030253..2031535hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381283
hg191283
hg181283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593370, nsv593369, nsv593368
Samples
Known GenesNAT8L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8907n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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