A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv982e199



Internal ID20124284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150953043..150965590hg38UCSC Ensembl
chr4:151874195..151886742hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3812548
hg1912548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675985, esv2663628, esv2670596
SamplesNA20281, NA18870, NA18520, NA19904, NA20278, NA18871, NA19209, NA18511, NA20299, NA20294, NA18516, HG01082, NA19834, NA19108, NA19236, NA18873, NA18868, NA20340, NA19914, NA19982, NA18508, NA19917, NA19107, HG01061, NA18856, NA20127, NA20282, NA19700, NA19190, NA19213, NA19129, NA19172, NA19189, NA20291, NA19703, NA20348, NA18498, NA18522, NA18502, NA19901, NA18487, NA19707, NA19921, NA20276, NA20332, NA19818, NA19099, NA19225, NA18924, NA18853, NA19204, NA18908
Known GenesLRBA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv982e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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