A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667745



Internal ID9933850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105784488..105784944hg38UCSC Ensembl
Outerchr8:105784117..105785314hg38UCSC Ensembl
Innerchr8:106796716..106797172hg19UCSC Ensembl
Outerchr8:106796345..106797542hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381198
hg191198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5408189, essv6460985, essv5419229, essv6292711, essv5424636, essv5627533, essv5755243, essv6046561, essv5748482, essv5496504, essv6014615, essv6169243, essv6011402, essv6499980, essv6353251, essv6433193, essv6285858, essv6144859, essv5443210, essv5982192, essv6079504, essv5981149, essv5610743, essv5748855, essv5817511, essv5580916, essv6569898, essv6434173, essv6500827, essv6009277, essv6033002, essv6153950, essv6268766, essv6243063, essv6233984, essv5474257, essv5626837, essv6323763, essv6251382, essv5827121, essv5754044, essv6361778, essv5738710, essv6342623, essv6227598, essv6019257, essv5512104, essv6196079, essv6195547, essv5734462, essv6347790, essv6178522, essv6125423, essv6513714, essv6469879, essv6298968, essv6282270, essv6488321, essv6420818, essv6019075, essv6062265, essv5555840, essv5515074, essv5934632, essv5831046, essv5464962, essv5694276, essv5875087, essv6216368, essv6581208, essv5689379, essv5721359, essv6475093, essv5926873, essv5858255, essv5636937, essv6211988, essv5628291, essv5621133, essv6395180, essv6059573, essv6276187, essv5950370, essv6078296, essv6573535, essv5494942, essv6124267, essv5953384, essv5637928, essv6399196, essv5869844, essv5864354, essv6283706, essv6184493, essv5867439, essv6440389, essv6044773, essv5854206, essv6202287, essv6056470, essv6081030, essv6060375, essv5486870, essv6102663, essv5720796, essv5505655, essv5902064, essv6098437, essv5500511, essv6146609, essv5931901, essv6585602, essv6141430, essv5488381, essv6019656, essv6200624, essv6057211, essv5585685, essv5978086, essv6020343, essv6261225, essv6545708, essv6245549, essv5606655, essv6319636, essv6220901, essv6132162, essv6084850, essv6509434, essv6193678, essv6192921, essv6366244, essv6077157, essv6372117, essv5464555, essv5794222, essv5564624, essv5836618
SamplesNA19394, NA18502, NA19700, NA19397, NA18924, NA19909, NA19332, NA18917, NA18486, NA20294, NA19355, NA19819, NA18504, NA20332, HG00737, HG00115, NA20346, NA19098, NA20356, NA19920, NA19107, NA19396, NA19381, NA19379, NA18519, NA19319, NA19201, NA19382, NA19315, HG01167, NA19119, NA18923, NA19198, NA19916, NA18916, NA19313, NA19138, NA18498, NA20287, NA20336, NA20291, NA19130, NA19404, NA18874, NA18868, NA19917, NA19137, NA20340, NA19372, NA19371, NA19238, NA19235, NA19207, NA19317, HG01440, NA19159, NA19901, NA18520, NA19239, NA19209, NA19456, NA20127, NA18867, NA19921, NA19451, NA19200, NA19908, NA19437, NA19403, NA19462, NA19347, NA19455, NA19236, NA18516, NA19982, NA18871, NA18907, HG01073, NA19461, NA19114, NA18499, NA18856, HG01101, NA19099, NA19338, NA19257, NA19452, NA19225, NA19469, NA19395, NA19625, NA18858, NA19436, HG01148, NA19390, NA18909, NA19834, NA19108, NA19256, NA19147, NA18517, NA20276, NA19712, NA19434, NA19473, NA19435, NA19331, NA19240, NA19835, NA19470, NA19311, NA19467, NA20281, NA20341, NA19818, NA19398, NA20348, NA19248, NA19438, NA19472, NA20334, NA19468, NA19713, NA19474, NA19093, NA20289, NA19102, NA19116, NA19711, NA19213, NA19430, NA18505, NA19129, NA19316, NA18522, NA19346, NA18487, NA19431
Known GenesZFPM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667745
Frequency
Sample Size1151
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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