A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv488e199



Internal ID22758261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24529606..24535265hg38UCSC Ensembl
chr16:24540927..24546586hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668750, esv2664056, esv2675316
SamplesNA19701, NA19703, NA19397, NA18924, HG01462, NA19204, NA18508, NA18486, NA20294, NA19355, NA19377, HG01461, NA19098, NA19920, NA19107, NA19396, NA19201, NA20586, NA19197, NA19404, NA18874, NA19137, NA19207, NA19172, NA19901, NA18520, NA20342, NA19445, NA18934, NA19982, NA18907, NA19114, NA18853, NA19099, NA18523, NA20296, NA19434, NA19835, NA19467, NA19360, NA19818, NA19328, NA20348, NA19223, NA19102, NA18873, NA19316, NA18522, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv488e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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