A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672835



Internal ID9938940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11108480..11108845hg38UCSC Ensembl
chr2:11248606..11248971hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6139140, essv6025072, essv6387158, essv6536197, essv5799341, essv6411019, essv6575876, essv6133119, essv6059848, essv5895019, essv6173764, essv5566723, essv5602732, essv6276266, essv5710014, essv5410372, essv5961002, essv5803095, essv5891073, essv5554343, essv5897091, essv5569732, essv6229414, essv5904174, essv5827357, essv6349671, essv5655895, essv5589614, essv6391804, essv5971142, essv5811994, essv5658949, essv5849646, essv6261129, essv6236716, essv6126510, essv5614011, essv6177887, essv5872389, essv5838651, essv6583384, essv6359574, essv6410526, essv5569370, essv5985019, essv5985462, essv5817269, essv6304632, essv6564571, essv5881689, essv6219309, essv5837508, essv5859437, essv5815935, essv6387801, essv5952775, essv5994275, essv6316145, essv5775544, essv5698912, essv6257587, essv6390875, essv5730401, essv6496433, essv5642151, essv6415135, essv5863516, essv6449678, essv6447265, essv5408171, essv6114921, essv5807884, essv5438955, essv6446204, essv6013765, essv6002580, essv5620028, essv5902990, essv5744829, essv6494091, essv6282996, essv6333985, essv5904903, essv6399215, essv5577741, essv6242481, essv5583282, essv6213299, essv6316123, essv6197383, essv6567201, essv5431868, essv6336288, essv6315250, essv6047953, essv5491117, essv6273486, essv5511260, essv5980581, essv6578437, essv6251349, essv6106923, essv5993248, essv5446539, essv6090976, essv5869602, essv5646025, essv6593045, essv5633651, essv6002400, essv6116474, essv5653673, essv6300706, essv5987263, essv5964277, essv6296768, essv6072825, essv5940685, essv6422687, essv5548587, essv5509750, essv6589910, essv5796970, essv6027497, essv5431682, essv6553833, essv5423460, essv6080677, essv5936544, essv5560949, essv6166463, essv5426560, essv6500936
SamplesHG00114, HG00542, NA12717, NA11830, HG00143, HG00142, NA18947, NA10851, NA19399, NA19914, HG00640, HG00318, NA19359, NA18545, NA12004, NA18596, NA19377, NA18530, NA18870, NA20356, NA18510, HG00337, NA07346, NA18940, NA18519, HG00272, HG00251, NA18567, NA18619, NA12891, HG00736, NA11992, NA19457, HG00247, NA18498, NA19130, NA18949, HG00158, NA20518, NA12156, NA06984, NA12044, NA11994, HG00427, HG00338, NA18557, HG01048, NA19209, HG00323, HG00419, NA11993, HG00108, NA20818, HG00133, NA19210, NA18613, NA18538, HG00268, NA19082, HG00282, NA19707, NA19070, HG01384, HG00245, HG00428, NA19152, NA12878, NA19391, HG00475, NA18516, HG00583, NA18579, NA18537, HG01102, HG00324, HG01073, NA18573, NA11919, HG00373, NA11894, HG00684, NA12249, NA18912, NA12892, HG00525, HG00140, HG00276, NA19225, NA18523, NA19395, NA12546, NA12043, NA18953, HG00611, HG00124, NA18542, NA12716, HG00254, NA18909, NA11881, HG00336, NA18961, NA18952, HG00625, NA19072, HG00136, HG00278, NA07051, NA20778, HG00607, NA19311, NA18943, HG01108, HG00256, NA06986, HG00269, NA19376, NA19438, HG00329, HG00342, HG00123, NA18609, NA18552, NA07056, NA11892, NA19463, NA18522, NA12154, HG01437, HG00437, NA19153, HG00581, NA18620
Known GenesFLJ33534
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672835
Frequency
Sample Size1151
Observed Gain0
Observed Loss133
Observed Complex0
Frequencyn/a


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