A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607849



Internal ID6994780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:327586..368712hg38UCSC Ensembl
chr6:327586..368712hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3841127
hg1941127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1159e214
Supporting Variantsessv12167048, essv12167018, essv12167042, essv12166991, essv12166988, essv12166986, essv12166977, essv12167028, essv12167041, essv12167027, essv12166985, essv12167040, essv12167039, essv12166978, essv12167037, essv12167033, essv12167026, essv12167011, essv12167017, essv12166990, essv12167008, essv12167003, essv12166975, essv12167049, essv12166993, essv12166992, essv12166984, essv12167020, essv12167035, essv12167034, essv12167030, essv12167036, essv12167047, essv12167031, essv12167014, essv12167002, essv12166997, essv12166982, essv12167000, essv12167044, essv12167005, essv12167022, essv12166995, essv12167010, essv12167024, essv12167043, essv12166998, essv12167012, essv12166989, essv12166981, essv12166994, essv12166976, essv12167009, essv12166979, essv12167032, essv12167045, essv12166999, essv12166983, essv12167016, essv12167013, essv12167023, essv12167046, essv12167019, essv12166980, essv12167001, essv12167021, essv12167007, essv12166987, essv12167004, essv12167029, essv12167015, essv12167025, essv12167006, essv12167038, essv12166996
SamplesNA19701, HG01521, NA11829, HG04202, HG02419, NA20813, NA20802, HG03115, HG00318, HG03280, HG01686, HG00341, HG00654, HG02536, HG02285, NA18969, HG02153, HG03757, NA20589, NA20320, HG02541, HG01492, NA18916, HG02299, NA19197, NA12762, NA21108, HG03830, NA12761, HG00277, HG03897, HG00379, NA19026, HG01932, HG00178, HG01605, HG00530, HG01603, HG02009, HG02402, NA18747, HG02136, NA19091, HG01595, HG02345, HG02380, HG01142, HG01607, HG01049, NA18536, NA12778, HG03991, HG00240, HG04200, NA18542, NA18952, HG02759, HG01362, HG00278, NA12873, HG01620, NA20544, NA20887, HG02181, HG03600, HG02971, HG01917, HG01935, HG03097, HG03733, HG01302, HG01111, HG03072, NA19065, HG03741
Known GenesDUSP22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607849
Frequency
Sample Size2504
Observed Gain75
Observed Loss0
Observed Complex0
Frequencyn/a


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