A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv155e199



Internal ID22757928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73614031..73622484hg38UCSC Ensembl
chr10:75373789..75382242hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg388454
hg198454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674103, esv2664189
SamplesNA18502, NA18924, NA18508, HG01188, NA18504, NA19190, NA19920, NA19107, NA19374, NA19373, NA18916, NA19138, NA18498, NA20287, NA19130, HG01134, NA19172, NA19189, HG01124, NA19462, NA19391, NA18910, NA18871, NA19114, NA19449, NA18499, NA19453, NA19099, NA18523, NA19395, NA19401, NA19440, NA19108, NA18517, NA19444, NA19439, NA19428, NA19467, NA18501, NA19093, NA19102, HG01377, NA18505, NA19129, NA18511, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv155e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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