A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv469e199



Internal ID22758242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97988265..97993462hg38UCSC Ensembl
chr15:98531495..98536692hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658355, esv2664222
SamplesNA18502, NA18861, NA19399, NA19914, NA19704, NA18486, NA19393, NA18504, NA18870, NA19920, NA19374, NA19373, NA19171, NA19448, NA19119, NA19197, NA19404, NA19720, NA20278, NA18868, NA19137, NA19172, NA19239, NA19209, NA19451, NA19210, NA19437, NA18934, NA19462, NA19347, NA19152, NA19982, NA18910, NA18907, HG01047, NA19114, NA18856, NA19452, NA19225, NA18523, NA19401, NA18909, NA19108, NA19434, NA19444, NA19380, NA19428, NA19324, NA19467, NA20348, NA19093, NA19213, NA19129, NA18511, NA18522, NA19153
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv469e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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