Variant Details

Variant: esv3303387

Internal ID

15150335

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr13:78010527..78010528	hg38	UCSC Ensembl
Inner	chr13:78010510..78010545	hg38	UCSC Ensembl
Outer	chr13:78010509..78010546	hg38	UCSC Ensembl
	chr13:78584662..78584663	hg19	UCSC Ensembl
Inner	chr13:78584645..78584680	hg19	UCSC Ensembl
Outer	chr13:78584644..78584681	hg19	UCSC Ensembl
	chr13:77482663..77482664	hg18	UCSC Ensembl
Inner	chr13:77482681..77482646	hg18	UCSC Ensembl
Outer	chr13:77482645..77482682	hg18	UCSC Ensembl

Cytoband

13q22.3

Allele length

Assembly	Allele length
hg38	285
hg19	285
hg18	285

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7835251, essv7801668, essv7771090, essv7787112, essv7798021, essv7822019, essv7813239, essv7809914, essv7789674, essv7834108, essv7811983, essv7793339, essv7822457, essv7832716, essv7831196, essv7827797, essv7819103, essv7835616, essv7812849, essv7823161, essv7825155, essv7800313, essv7806874, essv7775308, essv7822776, essv7775599, essv7794133, essv7777480, essv7805461, essv7829617, essv7787562, essv7827944, essv7828919, essv7783287, essv7791488, essv7808231, essv7790024, essv7823686, essv7797762, essv7778052, essv7809204, essv7777085, essv7825953, essv7833366, essv7773529, essv7807720, essv7821343, essv7817232, essv7805116, essv7789367, essv7790555, essv7816780, essv7806251, essv7830670, essv7809057, essv7801438, essv7820645, essv7798275, essv7831688, essv7819994, essv7780767, essv7819641, essv7774096, essv7811274, essv7781746, essv7773715, essv7799160, essv7814865, essv7785117, essv7797138, essv7833121, essv7815333, essv7813988, essv7811697, essv7786652, essv7804246, essv7773177, essv7783825, essv7799769, essv7830203, essv7836053, essv7806496, essv7771791, essv7810069, essv7796762, essv7800859, essv7794798, essv7792029, essv7779871, essv7778422, essv7798728, essv7803352, essv7781227, essv7810908, essv7802894, essv7786481, essv7818135

Samples

NA18502, NA12717, NA11830, NA11829, NA18592, NA18508, NA10851, NA12414, NA18980, NA18561, NA11920, NA11931, NA18603, NA12751, NA12004, NA18504, NA18959, NA18870, NA18526, NA12750, NA12155, NA07346, NA19005, NA18940, NA18519, NA12812, NA12891, NA18960, NA18942, NA18916, NA11992, NA11918, NA07347, NA18582, NA18571, NA12287, NA18964, NA18949, NA12761, NA19238, NA11994, NA19172, NA19239, NA12828, NA18973, NA11993, NA11831, NA10847, NA18951, NA12489, NA12003, NA12878, NA12872, NA18956, NA18871, NA18572, NA18948, NA19114, NA11894, NA12249, NA12892, NA18853, NA19099, NA18555, NA18523, NA18570, NA18858, NA12043, NA18953, NA18542, NA12716, NA18909, NA11881, NA19108, NA18961, NA19147, NA18517, NA18564, NA19240, NA07051, NA18943, NA07037, NA12763, NA18501, NA12749, NA19093, NA18609, NA19102, NA18552, NA19129, NA12006, NA18511, NA07000, NA12154, NA18562, NA12776, NA18965

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3303387

Frequency

Sample Size	185
Observed Gain	97
Observed Loss	0
Observed Complex	0
Frequency	n/a