A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv517e199



Internal ID20123819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732691..89733030hg38UCSC Ensembl
chr16:89799099..89799438hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674443, esv2675816
SamplesHG01357, HG00613, NA12154, HG00252, HG00318, NA11930, NA07037, NA20522, HG00619, NA18534, NA18530, HG01052, NA18952, HG00437, NA20516, HG01083, NA18612, NA18526, HG00310, NA18570, HG00261, NA18545, NA18603, NA11931, HG00614, NA19920, HG00698, HG00111, HG00280, HG00699, NA12044, HG01551, NA18943, NA18596, HG00543, HG00154, HG01048, NA18990, HG01047, NA18592, NA12761, NA12829, NA11894, NA18637, NA20336, NA20520, HG00276, NA20341, HG00662, HG00620, HG00653, NA18572, HG01066, HG00513, HG00524, HG00512, HG00534, NA18940, NA18582, HG00590, NA20756, NA19818, NA18577, HG00654, HG00422, NA18610, NA18611, NA11829, HG00324, HG00690, NA20528, NA18549, HG00473, HG00336, HG00476, NA20502, HG00345, NA19385, NA19750, HG00278
Known GenesZNF276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv517e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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