A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv518e199



Internal ID22758291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89914167..89914745hg38UCSC Ensembl
chr16:89980575..89981153hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673025, esv2671088
SamplesNA19394, NA12383, HG00442, NA19700, NA19055, HG00231, HG01389, HG01374, HG00151, HG00699, NA19819, NA19377, NA18959, NA18616, HG00654, NA19920, NA19446, NA19005, HG00702, NA18567, NA20769, HG00270, HG00185, HG00537, HG01134, NA20759, HG01067, NA19383, NA18617, NA19471, HG01440, NA19002, HG01198, HG01048, NA19445, NA19921, HG00739, HG00464, HG01136, NA18613, HG00731, HG00380, NA19077, NA19462, HG00190, HG00701, NA19236, NA19982, HG00583, NA12718, NA20126, NA19654, NA19000, NA19084, HG00157, NA19009, HG00152, NA18963, NA19318, NA19685, NA18953, NA19729, NA19440, NA12716, NA19473, NA18628, HG01551, NA19010, HG01375, NA19835, HG00607, NA19467, NA20516, HG01108, NA18615, NA19818, NA19078, HG00614, NA19060, HG00656, HG00342, NA20334, NA19716, NA19102, HG00698, NA20758, NA19780, NA18989, NA19004, HG01061, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv518e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


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