A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2666027

Internal ID9585446
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111403388..111407451hg38UCSC Ensembl
chr9:114165668..114169731hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5845544, essv6408022, essv6398351, essv5847063, essv6301171, essv6310395, essv5972429, essv6130756, essv6293498, essv6131445, essv5811246, essv6567926, essv5471839, essv5527991, essv5670514, essv6189171, essv5879024, essv5530616, essv5586017, essv5845045, essv5936025, essv6217288, essv6539932, essv5993325, essv5815211, essv6331462, essv5641732, essv5963804, essv6469976, essv5437659, essv6472512, essv5888649, essv6392587, essv6401568, essv5562257, essv6008885, essv6366331, essv6350466, essv5697854, essv5721077, essv6061586, essv6196897, essv5409516, essv5558633, essv5682259, essv5490785, essv5926722, essv6539749, essv6022068, essv5464484, essv5426141, essv6419212, essv5452836, essv5735034, essv5648262, essv6049800, essv6397258, essv6002676, essv5998948, essv5427753, essv5479434, essv6260642, essv5642918, essv5451216, essv5784984, essv6566504, essv6117383, essv5495236, essv6431254, essv5758969, essv5570736, essv6105857, essv6335399, essv5574213, essv5943786, essv6457651, essv5587636, essv6207096, essv6587660, essv6379510, essv6530236, essv5934902, essv6532660, essv6536494, essv6186941, essv5726688, essv6096837, essv6545982, essv5727480, essv6434054, essv5946403, essv5547973, essv5564762, essv5821418, essv5484334, essv5651749, essv6107731, essv6467983, essv6387572, essv5869928, essv6186215, essv5653556, essv5726347, essv6428832, essv6544699, essv5781223, essv6180917, essv6512152, essv6386447, essv5767228, essv6364140, essv5590593, essv5604663, essv5913714, essv5411780, essv5948485, 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
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2666027
Sample Size1151
Observed Gain0
Observed Loss124
Observed Complex0

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