A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671802



Internal ID9937907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2907165..2907421hg38UCSC Ensembl
Outerchr6:2907128..2907471hg38UCSC Ensembl
Innerchr6:2907399..2907655hg19UCSC Ensembl
Outerchr6:2907362..2907705hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6516233, essv5414418, essv5816092, essv5492419, essv6174143, essv6431459, essv5818473, essv5602546, essv5596726, essv6597090, essv6589238, essv5589048, essv6372621, essv6199406, essv6297976, essv5767969, essv6309027, essv5567467, essv6231355, essv6410338, essv6267154, essv5826939, essv6437021, essv5667623, essv5757722, essv5930168, essv5864316, essv6592736, essv5886013, essv6215500, essv6079018, essv6009178, essv5447450, essv5705834, essv5834141, essv6399778, essv5513944, essv5785270, essv6291287, essv6334134, essv5557413, essv6208354, essv5556864, essv5626944, essv6266904, essv6117183
SamplesNA12717, NA11995, HG00524, NA12843, HG00318, NA19190, NA18633, NA18510, HG00327, NA18489, NA19762, NA07347, HG00369, HG00334, NA18977, NA12889, HG00159, NA18557, HG00326, HG00530, NA19007, HG00443, HG00653, NA18534, NA18548, HG00284, HG00331, NA18912, NA19099, HG01334, HG00463, HG00246, NA19625, NA18858, NA20801, NA18909, HG00662, HG00111, HG00513, HG00478, NA19093, NA18505, HG00345, NA12154, NA18622, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671802
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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