A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659169



Internal ID9925274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39096102..39096362hg38UCSC Ensembl
chr8:38953621..38953881hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6078716, essv6445775, essv5829770, essv6231214, essv6286625, essv6168712, essv6028480, essv5878288, essv6128872, essv5633239, essv6425168, essv5715348, essv5653510, essv5536294, essv6400644, essv6297966, essv5886795, essv6515916, essv5846682, essv6377104, essv6104037, essv5884427, essv6312514, essv6224315, essv6245372, essv5695761, essv6574668, essv5903210, essv6294483, essv6343118, essv5941902, essv6492505, essv6388773, essv6223461, essv6086951, essv5745911, essv5982054, essv5661790, essv5596797, essv5800073, essv5448603, essv5854469, essv5430083, essv6123967, essv6523366, essv5581617, essv6091001, essv5978105, essv6401379, essv5815227, essv5751053, essv6425419, essv5493677, essv6467972, essv6407614, essv5534206, essv5849572, essv6413975, essv6026379, essv5915080, essv5849035, essv6584367, essv6513413, essv6082434, essv6403847, essv6298402, essv5528611, essv6075353, essv6376273, essv6104915, essv6570349, essv6210542, essv6524338, essv6129644, essv5998662, essv6301227, essv5871806, essv5476923, essv5461634, essv6345290, essv5536791, essv5459875, essv5642617, essv6254523, essv6020647, essv5620996, essv6466603, essv5944236, essv5432449, essv6429225, essv5944477, essv5517640, essv6553544, essv5819991, essv5980757, essv6277786, essv6238287, essv5968969, essv5562847, essv5418246, essv5812617, essv5899211, essv6270591, essv5565084, essv6221262, essv6080135, essv6211986, essv5862089, essv5580070, essv6277564, essv5935352, essv5478875, essv5450618, essv6367575, essv6129585, essv5921362, essv5833459, essv6022341, essv5906109, essv5862491, essv5978540, essv5805161, essv6370791, essv6478505
SamplesHG00626, HG01441, NA12717, HG00442, NA19700, HG00361, NA18592, HG00559, HG01052, NA18599, HG00315, NA20802, NA19777, HG00566, HG00150, HG00654, HG00261, NA18602, NA18988, HG00337, HG00663, NA18940, HG01070, HG00122, NA18597, HG00448, NA18567, NA12891, NA18558, HG00330, NA18547, NA19131, NA18618, HG00610, NA18574, NA12287, HG00334, NA19782, NA18949, HG00158, NA12761, HG01134, HG00236, NA20812, NA11932, NA18617, HG00422, HG00705, HG00309, NA19725, NA19239, HG00530, HG00419, HG00253, HG00543, HG00137, HG01183, HG01136, NA18951, NA18544, NA18605, NA19657, HG00557, NA12878, HG00657, HG00475, NA19663, NA18516, NA18637, HG00263, NA18579, NA12718, HG01149, HG00692, NA18537, NA18573, NA19000, NA18626, HG00404, HG00531, NA12829, HG00331, NA11894, HG00684, NA18532, HG00613, NA18555, HG00463, HG00246, NA18570, NA18593, NA18541, HG01204, NA18576, NA18546, NA12043, HG00124, NA18533, HG00254, HG00285, NA18543, HG00136, NA07051, NA20803, NA07037, HG00256, HG00662, HG00269, HG00125, HG00478, NA18971, HG00421, HG00342, NA19093, HG00123, HG00112, HG00698, HG00280, HG00343, NA18983, HG01125, NA07000, NA19065, NA19676
Known GenesADAM9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659169
Frequency
Sample Size1151
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


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