Variant Details

Variant: esv3305580

Internal ID

15152528

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:79503528..79503529	hg38	UCSC Ensembl
Inner	chr15:79503510..79503547	hg38	UCSC Ensembl
Outer	chr15:79503509..79503548	hg38	UCSC Ensembl
	chr15:79795870..79795871	hg19	UCSC Ensembl
Inner	chr15:79795852..79795889	hg19	UCSC Ensembl
Outer	chr15:79795851..79795890	hg19	UCSC Ensembl
	chr15:77582925..77582926	hg18	UCSC Ensembl
Inner	chr15:77582944..77582907	hg18	UCSC Ensembl
Outer	chr15:77582906..77582945	hg18	UCSC Ensembl

Cytoband

15q25.1

Allele length

Assembly	Allele length
hg38	291
hg19	291
hg18	291

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7835013, essv7807294, essv7794804, essv7815086, essv7811422, essv7806347, essv7827247, essv7792426, essv7777023, essv7772302, essv7823679, essv7819774, essv7807959, essv7835448, essv7807412, essv7797116, essv7798470, essv7783185, essv7832269, essv7790262, essv7813698, essv7787935, essv7816734, essv7779531, essv7832893, essv7821669, essv7806667, essv7829275, essv7791675, essv7777968, essv7833515, essv7799421, essv7783553, essv7771829, essv7777234, essv7808675, essv7811684, essv7775588, essv7825861, essv7814254, essv7831489, essv7801857, essv7809867, essv7796565, essv7786427, essv7784316, essv7793153, essv7829082, essv7790871, essv7780951, essv7785999, essv7781749, essv7836561, essv7775225, essv7803581, essv7782463, essv7794122, essv7778916, essv7805230, essv7805139, essv7801406, essv7815775, essv7795331, essv7793485, essv7802781, essv7809179, essv7834748, essv7810793, essv7830541, essv7812442, essv7831015, essv7772742, essv7770058, essv7821065, essv7815557, essv7817349, essv7797634, essv7788318, essv7788939, essv7789303, essv7774625, essv7773808, essv7780524, essv7786837, essv7798888, essv7802242, essv7825725, essv7824490, essv7826558, essv7794550, essv7787043, essv7829819, essv7817457, essv7810173, essv7832485, essv7810480, essv7795860, essv7789667, essv7805751, essv7796216, essv7814745, essv7822192, essv7785032, essv7825068, essv7808335, essv7804387

Samples

NA18502, NA12717, NA11830, NA18861, NA18592, NA18508, NA18980, NA18561, NA11920, NA11931, NA18603, NA12045, NA18545, NA18504, NA18959, NA19190, NA18870, NA18526, NA18510, NA12750, NA12155, NA07346, NA18944, NA18550, NA12812, NA18489, NA18558, NA18916, NA11992, NA11918, NA07347, NA18582, NA18571, NA12287, NA19138, NA18964, NA18949, NA12761, NA18970, NA12044, NA11994, NA19172, NA18973, NA18638, NA11831, NA18951, NA18605, NA12489, NA12003, NA12878, NA12872, NA18956, NA18516, NA18579, NA18871, NA18572, NA18907, NA18537, NA18566, NA18573, NA19114, NA11919, NA18499, NA11894, NA18856, NA12249, NA18912, NA19099, NA19257, NA18555, NA12144, NA18523, NA18570, NA18858, NA18593, NA18945, NA18576, NA12043, NA18608, NA18542, NA19108, NA18961, NA18952, NA19147, NA18517, NA18564, NA19240, NA12873, NA18943, NA12874, NA07037, NA12763, NA06986, NA19143, NA12749, NA18609, NA19102, NA18552, NA18505, NA19129, NA18511, NA07000, NA18562, NA12776, NA18965, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3305580

Frequency

Sample Size	185
Observed Gain	106
Observed Loss	0
Observed Complex	0
Frequency	n/a