A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv90e199



Internal ID22757863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203917767..203920763hg38UCSC Ensembl
chr1:203886895..203889891hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382997
hg192997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664594, esv2676203
SamplesNA19701, NA18924, NA19466, NA19399, NA19914, NA19332, NA18507, NA20816, NA19350, NA19355, NA18504, NA20332, NA19377, NA19107, NA19446, NA19382, NA18489, NA19448, NA19678, NA18923, HG00736, NA18498, NA19384, NA19130, NA19404, HG01069, NA18868, NA19372, NA19235, NA19385, NA19172, NA19471, NA19317, NA18908, NA19985, NA19921, NA19451, NA19908, NA19707, NA18934, NA19403, NA19347, HG01095, NA19455, NA19236, NA18910, NA18871, NA18907, NA18856, NA19453, NA18853, HG01497, NA19099, NA19257, NA19395, NA19436, NA19440, NA18909, NA19147, NA19434, NA19473, NA19334, NA19439, NA19470, NA19311, NA20281, NA19360, NA19376, NA19472, NA19468, NA19474, NA19102, NA18873, NA19116, NA19711, NA19430, NA19316, NA19463, NA18522, HG01191, NA19429, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv90e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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