A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3395081



Internal ID15242045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157547665..157547729hg38UCSC Ensembl
Innerchr6:157547648..157547746hg38UCSC Ensembl
Outerchr6:157547584..157547810hg38UCSC Ensembl
chr6:157968697..157968761hg19UCSC Ensembl
Innerchr6:157968680..157968778hg19UCSC Ensembl
Outerchr6:157968616..157968842hg19UCSC Ensembl
chr6:157888685..157888749hg18UCSC Ensembl
Innerchr6:157888766..157888668hg18UCSC Ensembl
Outerchr6:157888604..157888830hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3686e59
Supporting Variantsessv8933922, essv8933910, essv8933907, essv8933915, essv8933901, essv8933913, essv8933911, essv8933887, essv8933900, essv8933954, essv8933926, essv8933956, essv8933883, essv8933948, essv8933878, essv8933898, essv8933945, essv8933957, essv8933899, essv8933894, essv8933961, essv8933917, essv8933932, essv8933928, essv8933942, essv8933944, essv8933941, essv8933937, essv8933888, essv8933906, essv8933929, essv8933918, essv8933885, essv8933930, essv8933924, essv8933897, essv8933921, essv8933881, essv8933923, essv8933939, essv8933904, essv8933879, essv8933946, essv8933934, essv8933938, essv8933952, essv8933933, essv8933905, essv8933875, essv8933890, essv8933889, essv8933949, essv8933882, essv8933912, essv8933950, essv8933960, essv8933896, essv8933902, essv8933959, essv8933876, essv8933935, essv8933955, essv8933916, essv8933893, essv8933919, essv8933951, essv8933877, essv8933943, essv8933920, essv8933940, essv8933909, essv8933886, essv8933908, essv8933953, essv8933931, essv8933874, essv8933895, essv8933927, essv8933884
SamplesNA18502, NA12717, NA18947, NA11995, NA18861, NA18592, NA18508, NA10851, NA12414, NA18561, NA18507, NA11931, NA12045, NA18486, NA12751, NA18545, NA19190, NA18870, NA18526, NA12750, NA12155, NA07346, NA19005, NA18944, NA18940, NA18550, NA18519, NA18558, NA18547, NA11918, NA07347, NA19138, NA18949, NA12761, NA12156, NA11994, NA18520, NA11993, NA10847, NA18516, NA18579, NA18871, NA18572, NA18907, NA18537, NA19114, NA11919, NA18499, NA18856, NA18912, NA18853, NA19099, NA19257, NA19225, NA12144, NA18523, NA18593, NA12043, NA18608, NA18542, NA18909, NA11881, NA19108, NA18961, NA19147, NA18517, NA07051, NA18943, NA07037, NA18501, NA19093, NA19102, NA19116, NA18505, NA19129, NA18511, NA07000, NA18522, NA12154
Known GenesZDHHC14
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3395081
Frequency
Sample Size185
Observed Gain79
Observed Loss0
Observed Complex0
Frequencyn/a


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