A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666027



Internal ID9585446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111403388..111407451hg38UCSC Ensembl
chr9:114165668..114169731hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384064
hg194064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5845544, essv6408022, essv6398351, essv6301171, essv5847063, essv6310395, essv5972429, essv6293498, essv6130756, essv6131445, essv6567926, essv5811246, essv5471839, essv5527991, essv5670514, essv6189171, essv5879024, essv5530616, essv5586017, essv5845045, essv5936025, essv6217288, essv6539932, essv5993325, essv5815211, essv6331462, essv6469976, essv5963804, essv5641732, essv5437659, essv6472512, essv6392587, essv5888649, essv6401568, essv6008885, essv5562257, essv6366331, essv6350466, essv5697854, essv5721077, essv6061586, essv6196897, essv5409516, essv5682259, essv5558633, essv5490785, essv5926722, essv6539749, essv6022068, essv5464484, essv5426141, essv6419212, essv5735034, essv5452836, essv6049800, essv6397258, essv5648262, essv6002676, essv5998948, essv5427753, essv5479434, essv6260642, essv5642918, essv5784984, essv5451216, essv6566504, essv6117383, essv5495236, essv6431254, essv5758969, essv6335399, essv5570736, essv6105857, essv5574213, essv6457651, essv5943786, essv5587636, essv6207096, essv6587660, essv6379510, essv6530236, essv6536494, essv6532660, essv5934902, essv6186941, essv5726688, essv6096837, essv6545982, essv5727480, essv6434054, essv5946403, essv5564762, essv5547973, essv5821418, essv5484334, essv6107731, essv5651749, essv6467983, essv6387572, essv5869928, essv6186215, essv5653556, essv5726347, essv6428832, essv6544699, essv5781223, essv6180917, essv6512152, essv6386447, essv5767228, essv6364140, essv5590593, essv5604663, essv5913714, essv5948485, essv5411780, essv5723885, essv6371904, essv5915096, essv5438076, essv6043806, essv5592015, essv6501640, essv6370101
SamplesHG00613, NA18964, NA19152, NA19436, NA18605, HG00536, HG00607, NA18595, NA18630, NA19437, NA18612, NA19209, NA18501, NA19093, HG00449, NA19469, NA18550, NA18570, HG00707, NA19455, NA19430, NA19359, NA19338, NA19449, NA18573, HG00446, NA18541, HG01188, HG00581, HG00557, NA19257, HG00578, NA19701, NA19236, NA19355, NA19474, NA19084, NA18505, NA19472, HG00479, HG00247, HG00592, HG00635, NA19067, NA19383, HG01384, NA18536, NA18622, NA18623, NA19471, NA20757, HG00610, NA20754, NA20127, NA18638, NA19398, NA19429, NA19908, NA18547, NA19256, NA18593, NA19056, HG00403, NA19457, HG00662, NA18539, NA19190, NA19360, NA19377, NA19395, NA19080, NA19372, HG00653, NA19374, NA19703, NA19375, NA19384, NA18923, NA20826, NA19102, NA19713, NA18558, NA19901, NA18504, NA20818, NA18942, NA19332, NA18613, HG00524, HG00512, NA18562, NA19131, NA18910, NA18579, NA18940, NA19138, NA19376, HG00443, NA18907, NA18909, NA18867, NA19434, NA18602, NA19446, NA18533, NA18944, NA19225, NA19399, NA19160, NA18571, NA19916, NA18610, NA19130, NA19346, HG00442, NA19350, NA19473, HG00684, NA19448, HG00704, NA19385, NA18519, NA19058, HG00531
Known GenesKIAA0368
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666027
Frequency
Sample Size1151
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


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