Variant Details

Variant: esv3307759

Internal ID

15154707

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr2:2536159..2536160	hg38	UCSC Ensembl
Inner	chr2:2536141..2536178	hg38	UCSC Ensembl
Outer	chr2:2536140..2536179	hg38	UCSC Ensembl
	chr2:2539931..2539932	hg19	UCSC Ensembl
Inner	chr2:2539913..2539950	hg19	UCSC Ensembl
Outer	chr2:2539912..2539951	hg19	UCSC Ensembl
	chr2:2518938..2518939	hg18	UCSC Ensembl
Inner	chr2:2518957..2518920	hg18	UCSC Ensembl
Outer	chr2:2518919..2518958	hg18	UCSC Ensembl

Cytoband

2p25.3

Allele length

Assembly	Allele length
hg38	295
hg19	295
hg18	295

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7804880, essv7781053, essv7794063, essv7820372, essv7775353, essv7802287, essv7823167, essv7831964, essv7831129, essv7815344, essv7793583, essv7770879, essv7812037, essv7782454, essv7828798, essv7833953, essv7816841, essv7770180, essv7822876, essv7787831, essv7830201, essv7807004, essv7800185, essv7802994, essv7791069, essv7785058, essv7801900, essv7809902, essv7792822, essv7797217, essv7790509, essv7777210, essv7796026, essv7798604, essv7823532, essv7785778, essv7836187, essv7814814, essv7773185, essv7778449, essv7813379, essv7809473, essv7789062, essv7776930, essv7813714, essv7808085, essv7790001, essv7807662, essv7804648, essv7800620, essv7786524, essv7776334, essv7776429, essv7834580, essv7785218, essv7810250, essv7822291, essv7794721, essv7783546, essv7834258, essv7799120, essv7777774, essv7795294, essv7773791, essv7829565, essv7806735, essv7780622, essv7784056, essv7824477, essv7833363, essv7817078, essv7819486, essv7817823, essv7810668, essv7784106, essv7835116, essv7826778, essv7780068, essv7774889, essv7803318, essv7771242, essv7775847, essv7827100, essv7816197, essv7819957, essv7788412, essv7835659, essv7818697, essv7772722, essv7821159, essv7782878

Samples

NA18502, NA11830, NA18947, NA18592, NA12814, NA10851, NA18980, NA11920, NA11931, NA18603, NA12045, NA12751, NA18959, NA18870, NA18526, NA12750, NA12155, NA07357, NA07346, NA18563, NA19005, NA18944, NA18940, NA18550, NA12891, NA18558, NA18547, NA18960, NA18942, NA11918, NA07347, NA18571, NA19138, NA12761, NA18970, NA12156, NA12044, NA12815, NA12828, NA18973, NA11831, NA18951, NA18605, NA12489, NA12003, NA12878, NA12872, NA18579, NA18572, NA18948, NA12234, NA18537, NA18566, NA18573, NA19114, NA18856, NA12249, NA12892, NA18532, NA18853, NA18555, NA18523, NA18570, NA18593, NA18945, NA18576, NA12043, NA18608, NA18542, NA12716, NA11881, NA18961, NA18564, NA12873, NA07051, NA18943, NA12874, NA07037, NA18501, NA12749, NA18609, NA19116, NA18552, NA18505, NA19129, NA12006, NA07000, NA12154, NA18562, NA12776, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3307759

Frequency

Sample Size	185
Observed Gain	91
Observed Loss	0
Observed Complex	0
Frequency	n/a