A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623925



Internal ID7010781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79745548..79842753hg38UCSC Ensembl
chr10:81505304..81602509hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3897206
hg1997206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870194, essv13870201, essv13870182, essv13870174, essv13870202, essv13870142, essv13870181, essv13870195, essv13870121, essv13870163, essv13870120, essv13870113, essv13870169, essv13870127, essv13870134, essv13870185, essv13870175, essv13870190, essv13870167, essv13870188, essv13870189, essv13870187, essv13870116, essv13870128, essv13870191, essv13870157, essv13870146, essv13870159, essv13870148, essv13870144, essv13870183, essv13870115, essv13870112, essv13870196, essv13870136, essv13870166, essv13870147, essv13870118, essv13870151, essv13870198, essv13870149, essv13870135, essv13870205, essv13870129, essv13870193, essv13870114, essv13870162, essv13870154, essv13870123, essv13870164, essv13870161, essv13870203, essv13870130, essv13870156, essv13870138, essv13870170, essv13870132, essv13870199, essv13870200, essv13870150, essv13870197, essv13870126, essv13870172, essv13870173, essv13870168, essv13870125, essv13870140, essv13870177, essv13870119, essv13870122, essv13870152, essv13870204, essv13870153, essv13870133, essv13870186, essv13870111, essv13870141, essv13870179, essv13870178, essv13870158, essv13870160, essv13870139, essv13870171, essv13870124, essv13870184, essv13870155, essv13870165, essv13870145, essv13870176, essv13870137, essv13870117, essv13870131, essv13870180, essv13870192, essv13870206, essv13870143
SamplesHG01462, NA21089, NA12286, NA20274, HG03767, HG02275, NA19795, HG03941, HG00699, HG02277, HG02017, NA21115, HG00566, HG02271, NA19443, HG03999, HG01809, NA19067, NA19171, HG01325, NA19005, HG02690, HG04022, HG03757, HG01702, NA20890, HG00634, NA18960, HG02374, HG03234, HG01393, HG03793, NA12761, HG02067, HG03595, NA11994, HG03746, HG02082, HG03624, HG01892, HG04238, NA19725, NA18985, HG04029, HG01550, HG03844, NA18613, HG03908, HG00268, HG00266, HG01501, HG01187, HG03787, HG00332, HG04062, NA19462, NA20809, HG02057, HG03547, HG01515, HG04162, HG03491, NA18637, HG00500, HG03159, HG01880, HG01852, HG04177, HG01092, NA19654, HG00324, HG03871, NA11893, HG02048, HG02121, HG04063, HG01705, HG01708, HG03755, HG02127, HG00445, HG02330, HG01190, NA18559, HG01174, NA20888, HG00672, NA18631, HG03863, NA19755, NA19316, HG03931, HG02006, HG00978, HG00553, HG03864
Known GenesLOC642361
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623925
Frequency
Sample Size2504
Observed Gain0
Observed Loss96
Observed Complex0
Frequencyn/a


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