Variant Details

Variant: esv3305207

Internal ID

15152155

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:59225134..59225135	hg38	UCSC Ensembl
Inner	chr10:59225115..59225154	hg38	UCSC Ensembl
Outer	chr10:59225114..59225155	hg38	UCSC Ensembl
	chr10:60984894..60984895	hg19	UCSC Ensembl
Inner	chr10:60984875..60984914	hg19	UCSC Ensembl
Outer	chr10:60984874..60984915	hg19	UCSC Ensembl
	chr10:60654900..60654901	hg18	UCSC Ensembl
Inner	chr10:60654920..60654881	hg18	UCSC Ensembl
Outer	chr10:60654880..60654921	hg18	UCSC Ensembl

Cytoband

10q21.1

Allele length

Assembly	Allele length
hg38	303
hg19	303
hg18	303

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7806101, essv7785533, essv7835920, essv7807535, essv7805166, essv7836241, essv7810715, essv7828757, essv7800959, essv7773588, essv7787214, essv7782796, essv7771449, essv7816730, essv7815302, essv7813728, essv7800364, essv7783195, essv7781876, essv7798232, essv7774807, essv7819454, essv7813399, essv7807279, essv7833718, essv7827241, essv7795943, essv7773476, essv7809637, essv7789461, essv7828884, essv7778185, essv7832315, essv7817631, essv7777269, essv7831184, essv7797834, essv7793223, essv7804673, essv7824243, essv7794803, essv7784901, essv7814689, essv7788085, essv7794224, essv7779899, essv7771762, essv7792733, essv7818466, essv7826380, essv7823841, essv7776124, essv7812177, essv7785726, essv7819890, essv7824841, essv7784169, essv7770090, essv7790239, essv7790784, essv7798773, essv7780718, essv7787778, essv7809715, essv7835584, essv7829593, essv7777690, essv7808060, essv7804206, essv7811752, essv7802679, essv7834421, essv7810334, essv7782066, essv7801326, essv7788835, essv7780856, essv7775635, essv7825468, essv7817155, essv7799294, essv7771332, essv7772502, essv7812623, essv7789009, essv7797721, essv7793483, essv7772780, essv7796783, essv7776995, essv7826688, essv7821225, essv7821558, essv7805533, essv7778965, essv7827597, essv7821738, essv7775327, essv7802740, essv7803654, essv7781219, essv7794385, essv7796152, essv7835155, essv7822607, essv7818745, essv7791622, essv7820050, essv7808753, essv7822449, essv7820450, essv7830474, essv7770542

Samples

NA18502, NA19141, NA12717, NA11995, NA11829, NA18861, NA18592, NA12814, NA10851, NA12414, NA18980, NA18561, NA18507, NA11920, NA11931, NA18603, NA12045, NA12751, NA18545, NA18504, NA18526, NA18510, NA12750, NA12155, NA07357, NA07346, NA18563, NA19005, NA18944, NA18940, NA18550, NA12812, NA18489, NA12891, NA18558, NA18960, NA11992, NA11918, NA18582, NA18571, NA12287, NA18498, NA18964, NA18949, NA12761, NA12044, NA11994, NA19172, NA12815, NA18520, NA12828, NA18973, NA18638, NA11993, NA11831, NA10847, NA18951, NA18605, NA12003, NA12878, NA12872, NA18579, NA18572, NA18948, NA12234, NA18537, NA18566, NA18573, NA19114, NA11919, NA18499, NA11894, NA11840, NA12249, NA12892, NA18532, NA18555, NA19225, NA12144, NA18523, NA18570, NA18858, NA18593, NA18945, NA18576, NA12043, NA18608, NA18542, NA12716, NA11881, NA19108, NA18952, NA18517, NA18564, NA12873, NA07051, NA18943, NA12874, NA07037, NA06986, NA18501, NA12749, NA19093, NA18609, NA19102, NA18552, NA18505, NA19129, NA07000, NA12154, NA18562, NA18965, NA18577

Known Genes

PHYHIPL

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3305207

Frequency

Sample Size	185
Observed Gain	113
Observed Loss	0
Observed Complex	0
Frequency	n/a