A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673884



Internal ID9593303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41257715..41258003hg38UCSC Ensembl
chr20:39886355..39886643hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6337631, essv6563721, essv6018520, essv5643611, essv6449366, essv6400436, essv6002102, essv5479772, essv5553250, essv5540663, essv5687119, essv6192537, essv6287121, essv6066222, essv5711661, essv5765496, essv5618351, essv5733430, essv6586114, essv5450597, essv5709231, essv6098334, essv6171020, essv6576644, essv6454539, essv6156560, essv5802868, essv6239135, essv6466097, essv5633889, essv5870220, essv5520122, essv5744695, essv6232647, essv6361606, essv6247017, essv5564940, essv5728386, essv5871127, essv6533791, essv5970796, essv5907894, essv5432785, essv5517846, essv6342103, essv5804992, essv5478255, essv5520682, essv6227348, essv5915575, essv5785058, essv6135386, essv5740765, essv6539209, essv5902194, essv5927056, essv5483010, essv6195085, essv6423572, essv5946278, essv5670198, essv5590535, essv5487573, essv6041293, essv5644670, essv5722378, essv5614405, essv5551367, essv6037171, essv5844288, essv6242499, essv6540028, essv5900394, essv6027719, essv6176606, essv5848074, essv6260533, essv6401165, essv5771129, essv6072833, essv5546437, essv6138487, essv5967980, essv5897571
SamplesHG01441, NA18964, NA19312, NA19445, NA19625, NA19436, HG00536, HG01440, NA20503, HG01052, NA19819, HG00369, NA19311, NA20531, HG00310, HG00261, HG01079, NA20294, NA19359, HG00139, HG01188, HG00280, HG01171, NA18868, NA20340, HG00269, HG00342, NA19463, HG01140, HG01375, NA19390, NA19197, NA18990, HG01047, NA19396, NA20127, NA19398, NA19774, HG00125, NA19985, NA20282, NA20520, HG00243, HG00284, NA20341, HG01497, NA19213, HG00267, NA19189, NA19372, NA19703, NA19375, NA19384, NA18504, NA19704, HG00740, HG00524, HG00512, NA19707, NA19328, NA19376, NA19391, NA20276, NA18867, NA19403, NA18565, HG00138, NA20289, NA19818, NA19446, HG00530, NA20317, NA19327, NA12399, HG00142, NA18924, HG01108, HG00324, HG00183, NA19385, NA18519, HG00312, HG00327, HG00361
Known GenesZHX3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673884
Frequency
Sample Size1151
Observed Gain0
Observed Loss84
Observed Complex0
Frequencyn/a


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