A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305212



Internal ID15152160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882870..82882871hg38UCSC Ensembl
Innerchr15:82882853..82882883hg38UCSC Ensembl
Outerchr15:82882852..82882883hg38UCSC Ensembl
chr15:83551622..83551623hg19UCSC Ensembl
Innerchr15:83551605..83557690hg19UCSC Ensembl
Outerchr15:83551604..83557691hg19UCSC Ensembl
chr15:81348676..81348677hg18UCSC Ensembl
Innerchr15:81348694..81348659hg18UCSC Ensembl
Outerchr15:81348658..81348695hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386062
hg196062
hg186062
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7789296, essv7783748, essv7831151, essv7832970, essv7782378, essv7803837, essv7800909, essv7805464, essv7825003, essv7801986, essv7776514, essv7790504, essv7825966, essv7787843, essv7821385, essv7808166, essv7816181, essv7771563, essv7770667, essv7835453, essv7773775, essv7798264, essv7783264, essv7814452, essv7811265, essv7794330, essv7809899, essv7824647, essv7797650, essv7829898, essv7815662, essv7792402, essv7796920, essv7771065, essv7777180, essv7821809, essv7780880, essv7804856, essv7799539, essv7816731, essv7772446, essv7812506, essv7777672, essv7828823, essv7813719, essv7801231, essv7785137, essv7806270, essv7811599, essv7794737, essv7784347, essv7781594, essv7804347, essv7813355, essv7803013, essv7819638, essv7832045, essv7806762, essv7799929, essv7793107, essv7831257, essv7833856, essv7793885, essv7793540, essv7827791
SamplesNA12717, NA11995, NA11829, NA18592, NA18508, NA12814, NA10851, NA11920, NA11931, NA18603, NA18486, NA18545, NA18504, NA19190, NA18870, NA18526, NA12750, NA12155, NA12812, NA18489, NA11992, NA11918, NA07347, NA19138, NA18498, NA12761, NA12156, NA11994, NA12815, NA19239, NA18973, NA18638, NA11993, NA11831, NA18951, NA18605, NA12489, NA12872, NA18871, NA19114, NA18499, NA12249, NA18912, NA12892, NA19099, NA19225, NA12144, NA18858, NA12716, NA11881, NA18961, NA19147, NA19240, NA07051, NA07037, NA19143, NA12749, NA19093, NA19116, NA18552, NA18505, NA12006, NA18511, NA07000, NA18562
Known GenesHOMER2
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305212
Frequency
Sample Size185
Observed Gain65
Observed Loss0
Observed Complex0
Frequencyn/a


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