A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666537



Internal ID9932642
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 Variantsdgv1405e199
Supporting Variantsessv5661275, essv6052644, essv6450042, essv5782350, essv5741478, essv5726984, essv5445003, essv6008856, essv6547697, essv6227564, essv6121016, essv6532879, essv6319955, essv6082181, essv6228491, essv5652408, essv6394374, essv6216785, essv5580567, essv5592627, essv6461947, essv5669404, essv5620588, essv5554325, essv5953738, essv6517926, essv6354230, essv5940448, essv5395757, essv5636200, essv5761823, essv5422632, essv6137571, essv6305329, essv5605644, essv6098087, essv5581635, essv5695280, essv5601742, essv5814843, essv6045105, essv5857334, essv5686842, essv6118361, essv6080671
SamplesHG00442, NA19648, NA19055, NA18947, NA19066, NA18980, HG01374, NA18959, NA19068, NA18940, HG00448, NA18567, NA20795, NA18619, NA18558, NA18547, HG01492, HG01134, HG01080, HG01067, HG00705, NA18638, NA18605, NA12489, HG01498, NA19788, NA19064, NA18537, NA19654, NA18566, HG01073, NA18532, NA18963, NA18541, NA18542, NA18533, HG00734, HG01375, NA18610, HG01342, HG01491, NA19779, NA18549, NA18965, NA18577
Known GenesCD99L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666537
Frequency
Sample Size1151
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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