A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1405e199



Internal ID20124707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150769674..150769787hg38UCSC Ensembl
chrX:149938147..149938260hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666537, esv2662036
SamplesNA12489, HG00734, NA18605, HG01072, HG00705, HG01342, HG01083, NA18612, HG00614, NA19788, HG01492, NA18947, HG01491, NA18542, NA18541, NA18546, HG00581, NA18963, NA19648, HG01134, NA18965, NA18557, NA19654, HG00543, HG01375, NA18566, NA19068, HG01061, NA18638, NA19066, NA18959, NA18609, NA18547, HG00584, NA19055, NA18537, NA18633, NA20795, HG01073, NA18558, HG00501, HG01356, HG01080, NA18613, HG00512, HG00525, NA18543, NA18940, NA18619, HG00443, NA18567, HG00448, NA18577, NA18533, NA19064, NA18610, HG01498, NA18532, NA18549, HG00442, HG01374, HG00473, HG00684, NA19779, NA18980, HG01067
Known GenesCD99L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1405e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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