A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666469



Internal ID9932574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1611569..1611971hg38UCSC Ensembl
chrX:1730462..1730864hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5396067, essv5440723, essv6080492, essv6435283, essv6315125, essv6553604, essv6135283, essv5543868, essv5413370, essv6451018, essv6391990, essv5447873, essv6160028, essv6164488, essv5966008, essv5513711, essv6304778, essv5605281, essv6084502, essv5791061, essv5760600, essv5424383, essv6026123, essv5396549, essv5525760, essv6503734, essv6581639, essv6127278, essv6261449, essv5819521, essv5989708, essv5737764, essv5579911, essv5402064, essv5846880, essv6227991, essv5461719, essv5773304, essv5940317, essv6535195, essv6045280, essv5498352, essv6020362, essv5670592, essv6327477, essv5659771, essv5506950, essv6346947, essv6395477, essv5869846, essv5746376, essv5753510, essv6360022, essv5410567, essv5536123, essv5988310, essv5525709, essv6371130, essv6549246, essv6013836, essv6456586, essv5872811, essv6242155, essv6031733, essv5535853, essv5660815, essv5768990, essv6164470, essv6257754, essv6261862, essv5959739, essv6420573, essv6289938, essv5967410, essv5966528, essv5619783, essv5542408, essv6037281, essv5861789, essv5615728, essv6551920, essv5781186, essv5446101, essv5430161, essv6473782, essv5709464, essv5983615, essv5784402, essv6345497, essv6531130, essv6399227, essv5861437, essv5786031, essv5545766, essv5526032, essv6571143, essv5766670, essv5549355, essv5407757, essv5808749
SamplesHG00608, HG00524, NA19399, HG01052, NA18565, HG01079, NA18599, NA19819, HG00179, HG01051, HG01140, HG00327, HG01366, HG01070, HG00501, NA18595, NA19678, HG00702, HG00689, HG00448, NA18567, NA18574, NA19457, HG00247, NA19384, NA19130, HG00512, HG00281, HG00277, HG01080, HG00683, HG01170, HG00236, NA18868, HG01072, NA19385, NA18557, HG01048, HG01133, NA19445, HG00326, HG00323, HG00530, HG00253, NA19451, NA18638, NA18614, HG00137, NA18544, NA19437, HG00268, HG00183, NA19082, HG00282, NA19077, HG00428, HG00436, HG00320, NA19064, HG01102, HG00324, HG01073, HG00690, HG01383, NA19452, HG00704, NA18536, NA19436, NA19401, HG00124, NA18542, HG00285, HG00625, NA19712, HG00357, HG00136, NA18941, HG00278, HG01174, HG01375, HG00607, NA19428, NA19360, HG00269, NA19818, HG00707, HG00513, HG00421, HG00342, HG01055, HG00343, HG01377, NA19430, HG01125, HG00628, HG00345, NA19463, NA18623, NA18549, HG00437
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666469
Frequency
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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