A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619836



Internal ID6660022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17257679..17263736hg38UCSC Ensembl
Innerchr9:17258179..17263236hg38UCSC Ensembl
Outerchr9:17256679..17264736hg38UCSC Ensembl
chr9:17257677..17263734hg19UCSC Ensembl
Innerchr9:17258177..17263234hg19UCSC Ensembl
Outerchr9:17256677..17264734hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg386058
hg196058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13412015, essv13412003, essv13411979, essv13411994, essv13412011, essv13412023, essv13412026, essv13412006, essv13412024, essv13411993, essv13411966, essv13412036, essv13412041, essv13411991, essv13412030, essv13412010, essv13411976, essv13411987, essv13412004, essv13412042, essv13411968, essv13411983, essv13412038, essv13411973, essv13412002, essv13412005, essv13411977, essv13411986, essv13412017, essv13412031, essv13411990, essv13411970, essv13412007, essv13411978, essv13412035, essv13411963, essv13412008, essv13412033, essv13411969, essv13412009, essv13412025, essv13412029, essv13412000, essv13412018, essv13412047, essv13412020, essv13412045, essv13412039, essv13412028, essv13412022, essv13411975, essv13412014, essv13411989, essv13412016, essv13412044, essv13412001, essv13411995, essv13412019, essv13411999, essv13412013, essv13411996, essv13412034, essv13412040, essv13411961, essv13412012, essv13411985, essv13412046, essv13412049, essv13411980, essv13411998, essv13412048, essv13411988, essv13411974, essv13411997, essv13411971, essv13411982, essv13411981, essv13412050, essv13411962, essv13412037, essv13411984, essv13411965, essv13412043, essv13412032, essv13411967, essv13412021, essv13411964, essv13412052, essv13411972, essv13412051, essv13412027, essv13411992
SamplesNA20281, HG01813, HG03121, HG02250, HG02108, NA19031, HG03064, HG01811, HG02164, HG02816, NA18501, HG02896, NA19149, NA19455, NA20294, HG02979, NA19430, HG03057, NA19317, HG02974, HG02014, HG01816, HG03046, HG02946, NA19338, HG02944, NA18865, HG02508, HG03111, HG00683, HG02676, HG03103, NA19378, HG02274, HG02760, HG03548, HG01101, NA18873, HG02895, HG02402, HG03162, NA19914, HG03461, HG03193, HG03575, HG00593, NA19443, HG02568, HG02703, NA18856, HG00628, NA19397, HG02643, HG03520, HG02595, NA18539, HG00867, HG03085, NA19129, HG02768, HG02807, HG02429, HG02938, HG02502, HG02052, HG02536, HG02624, HG03303, NA20357, HG02923, HG01799, HG03367, HG03556, HG03198, NA18864, NA19749, HG02589, HG03074, NA18917, HG03369, HG03077, HG01108, HG02353, HG02721, HG03060, HG02798, HG00598, HG03517, HG02505, NA18519, HG03689, HG02610
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619836
Frequency
Sample Size2504
Observed Gain0
Observed Loss92
Observed Complex0
Frequencyn/a


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