A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669800



Internal ID9935905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:129616..202022hg38UCSC Ensembl
Outerchr6:129245..202392hg38UCSC Ensembl
Innerchr6:129616..202022hg19UCSC Ensembl
Outerchr6:129245..202392hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3873148
hg1973148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5856657, essv5866298, essv6014217, essv6187975, essv5424137, essv5556172, essv5627289, essv5581989, essv6311238, essv6522573, essv5819585, essv5471616, essv6336303, essv6025965, essv5412212, essv6325452, essv6058728, essv5447859, essv5738157, essv6123751, essv5795190, essv5948084, essv5734894, essv5689591, essv5923634, essv5467881, essv6081327, essv5665308, essv5705573, essv6332925, essv6059912, essv5923991, essv5792306, essv6071831, essv5865807, essv5617048, essv5866506, essv5975882, essv6291608, essv5727395, essv6466049, essv6559297, essv6307129, essv5510459, essv5765360, essv5619841, essv6342919, essv5660067, essv5792403, essv6558806, essv5967385, essv6121726, essv5865757, essv5689426, essv6296122, essv5738362, essv6529127, essv6148685, essv5835334, essv6455061, essv6151253, essv6012784, essv6367662, essv6548817, essv6323433, essv6541202, essv6320609, essv6245657, essv5686723, essv5553943, essv6297274, essv6382290, essv6090640, essv5677921, essv5450060, essv5794606, essv5958834, essv5555017, essv5919306, essv5751474, essv5518848, essv6316616, essv6304831, essv6101377
SamplesNA12383, NA12717, NA11830, NA12842, NA12286, NA11995, NA11829, NA10851, NA12273, NA12414, NA12843, NA11920, NA11933, NA11931, NA12045, NA12751, NA12004, NA12340, NA12058, NA12400, NA12750, NA12399, NA12155, NA07357, NA12413, NA12341, NA12813, NA07346, NA12348, NA11992, NA07048, NA11918, NA07347, NA12283, NA12287, NA12761, NA11930, NA12282, NA12275, NA12156, NA06984, NA11932, NA12044, NA11994, NA12828, NA11993, NA11831, NA10847, NA12777, NA12489, NA12342, NA12003, NA11919, NA12829, NA11893, NA11894, NA12249, NA06989, NA12827, NA12144, NA12778, NA12546, NA12043, NA12716, NA11881, NA12775, NA12272, NA07051, NA12046, NA07037, NA12763, NA12347, NA06986, NA06994, NA12749, NA12830, NA11843, NA07056, NA11892, NA12006, NA07000, NA12154, NA12776, NA11832
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669800
Frequency
Sample Size1151
Observed Gain0
Observed Loss84
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer